Method for the generation of compact TALE-nucleases and uses thereof

ABSTRACT

The present invention relates to a method for the generation of compact Transcription Activator-Like Effector Nucleases (TALENs) that can efficiently target and process double-stranded DNA. More specifically, the present invention concerns a method for the creation of TALENs that consist of a single TALE DNA binding domain fused to at least one catalytic domain such that the active entity is composed of a single polypeptide chain for simple and efficient vectorization and does not require dimerization to target a specific single double-stranded DNA target sequence of interest and process DNA nearby said DNA target sequence. The present invention also relates to compact TALENs, vectors, compositions and kits used to implement the method.

FIELD OF THE INVENTION

The present invention relates to a method for the generation of compact Transcription Activator-Like Effector Nucleases (TALENs) that can efficiently target and process double-stranded DNA. More specifically, the present invention concerns a method for the creation of TALENs that consist of a single TALE DNA binding domain fused to at least one catalytic domain such that the active entity is composed of a single polypeptide chain for simple and efficient vectorization and does not require dimerization to target a specific single double-stranded DNA target sequence of interest and process DNA nearby said DNA target sequence. The present invention also relates to compact TALENs, vectors, compositions and kits used to implement the method.

BACKGROUND OF THE INVENTION

Mammalian genomes constantly suffer from various types of damage, of which double-strand breaks (DSBs) are considered the most dangerous (Haber 2000). Repair of DSBs can occur through diverse mechanisms that can depend on cellular context. Repair via homologous recombination (HR) is able to restore the original sequence at the break. Because of its strict dependence on extensive sequence homology, this mechanism is suggested to be active mainly during the S and G2 phases of the cell cycle where the sister chromatids are in close proximity (Sonoda, Hochegger et al. 2006). Single-strand annealing (SSA) is another homology-dependent process that can repair DSBs between direct repeats and thereby promotes deletions (Paques and Haber 1999). Finally, non-homologous end joining (NHEJ) of DNA is a major pathway for the repair of DSBs that can function throughout the cell cycle and does not depend on homologous recombination (Moore and Haber 1996; Haber 2008). NHEJ seems to comprise at least two different components: (i) a pathway that consists mostly in the direct re-joining of DSB ends, and which depends on the XRCC4, Lig4 and Ku proteins, and; (ii) an alternative NHEJ pathway, which does not depend on XRCC4, Lig4 and Ku, and is especially error-prone, resulting mostly in deletions, with the junctions occurring between micro-homologies (Frank, Sekiguchi et al. 1998; Gao, Sun et al. 1998; Guirouilh-Barbat, Huck et al. 2004; Guirouilh-Barbat, Rass et al. 2007; Haber 2008; McVey and Lee 2008).

Homologous gene targeting (HGT), first described over 25 years ago (Hinnen, Hicks et al. 1978; Orr-Weaver, Szostak et al. 1981; Orr-Weaver, Szostak et al. 1983; Rothstein 1983), was one of the first methods for rational genome engineering and remains to this day a standard for the generation of engineered cells or knock-out mice (Capecchi 2001). An inherently low efficiency has nevertheless prevented it from being used as a routine protocol in most cell types and organisms. To address these issues, an extensive assortment of rational approaches has been proposed with the intent of achieving greater than 1% targeted modifications. Many groups have focused on enhancing the efficacy of HGT, with two major disciplines having become apparent: (i) so-called “matrix optimization” methods, essentially consisting of modifying the targeting vector structure to achieve maximal efficacy, and; (ii) methods involving additional effectors to stimulate HR, generally sequence-specific endonucleases. The field of matrix optimization has covered a wide range of techniques, with varying degrees of success (Russell and Hirata 1998; Inoue, Dong et al. 2001; Hirata, Chamberlain et al. 2002; Taubes 2002; Gruenert, Bruscia et al. 2003; Sangiuolo, Scaldaferri et al. 2008; Bedayat, Abdolmohamadi et al. 2010). Stimulation of HR via nucleases, on the other hand, has repeatedly proven efficient (Paques and Duchateau 2007; Carroll 2008).

For DSBs induced by biological reagents, e.g. meganucleases, ZFNs and TALENs (see below), which cleave DNA by hydrolysis of two phosphodiester bonds, the DNA can be rejoined in a seamless manner by simple re-ligation of the cohesive ends. Alternatively, deleterious insertions or deletions (indels) of various sizes can occur at the breaks, eventually resulting in gene inactivation (Liang, Han et al. 1998; Lloyd, Plaisier et al. 2005; Doyon, McCammon et al. 2008; Perez, Wang et al. 2008; Santiago, Chan et al. 2008; Kim, Lee et al. 2009; Yang, Djukanovic et al. 2009). The nature of this process, which does not rely on site-specific or homologous recombination, gives rise to a third targeted approach based on endonuclease-induced mutagenesis. This approach, as well as the related applications, may be simpler than those based on homologous recombination in that (a) one does not need to introduce a repair matrix, and; (b) efficacy will be less cell-type dependant (in contrast to HR, NHEJ is probably active throughout the cell cycle (Delacote and Lopez 2008). Targeted mutagenesis based on NEHJ has been used to trigger inactivation of single or even multiple genes in immortalized cell lines (Cost, Freyvert et al. 2010; Liu, Chan et al. 2010). In addition, this method opens new perspectives for organisms in which the classical HR-based gene knock-out methods have proven inefficient, or at least difficult to establish (Doyon, McCammon et al. 2008; Geurts, Cost et al. 2009; Shukla, Doyon et al. 2009; Yang, Djukanovic et al. 2009; Gao, Smith et al. 2010; Mashimo, Takizawa et al. 2010; Menoret, Iscache et al. 2010).

Over the last 15 years, the use of meganucleases to successfully induce gene targeting has been well documented, starting from straightforward experiments involving wild-type I-SceI to more refined work involving completely re-engineered enzymes (Stoddard, Scharenberg et al. 2007; Galetto, Duchateau et al. 2009; Marcaida, Munoz et al. 2010; Arnould, Delenda et al. 2011). Meganucleases, also called homing endonucleases (HEs), can be divided into five families based on sequence and structure motifs: LAGLIDADG, GIY-YIG, HNH, His-Cys box and PD-(D/E)XK (Stoddard 2005; Zhao, Bonocora et al. 2007). Structural data are available for at least one member of each family. The most well studied family is that of the LAGLIDADG proteins, with a considerable body of biochemical, genetic and structural work having established that these endonucleases could be used as molecular tools (Stoddard, Scharenberg et al. 2007; Arnould, Delenda et al. 2011). Member proteins are composed of domains that adopt a similar αββαββα fold, with the LAGLIDADG motif comprising the terminal region of the first helix and not only contributing to a bipartite catalytic center but also forming the core subunit/subunit interaction (Stoddard 2005). Two such α/β domains assemble to form the functional protein, with the β-strands in each creating a saddle-shaped DNA binding region. The spatial separation of the catalytic center with regions directly interacting with the DNA has allowed for specificity re-engineering (Seligman, Chisholm et al. 2002; Sussman, Chadsey et al. 2004; Arnould, Chames et al. 2006; Doyon, Pattanayak et al. 2006; Rosen, Morrison et al. 2006; Smith, Grizot et al. 2006; Arnould, Perez et al. 2007). In addition, whereas all known LAGLIDADG proteins analyzed to date act as “cleavases” to cut both strands of the target DNA, recent progress has been made in generating “mega-nickases” that cleave only one strand (Niu, Tenney et al. 2008; McConnell Smith, Takeuchi et al. 2009). Such enzymes can in principle provide similar levels of targeted induced HR with a minimization in the frequency of NHEJ.

Although numerous engineering efforts have focused on LAGLIDADG HEs, members from two other families, GIY-YIG and HNH, are of particular interest. Biochemical and structural studies have established that in both families, member proteins can adopt a bipartite fold with distinct functional domains: (1) a catalytic domain responsible mainly for DNA cleavage, and; (2) a DNA-binding domain to provide target specificity (Stoddard 2005; Marcaida, Munoz et al. 2010). The related GIY-YIG HEs I-TevI and I-BmoI have been exploited to demonstrate the interchangeability of the DNA-binding region for these enzymes (Liu, Derbyshire et al. 2006). Analysis of the I-BasI HE revealed that although the N-terminal catalytic domain belongs to the HNH family, the C-terminal DNA-binding region resembles the intron-encoded endonuclease repeat motif (IENR1) found in endonucleases of the GIY-YIG family (Landthaler and Shub 2003). The catalytic head of I-BasI has sequence similarity to those of the HNH HEs I-HmuI, I-HmuII and I-TwoI, all of which function as strand-specific nickases (Landthaler, Begley et al. 2002; Landthaler and Shub 2003; Landthaler, Lau et al. 2004; Shen, Landthaler et al. 2004; Landthaler, Shen et al. 2006).

Whereas the above families of proteins contain sequence-specific nucleases, the HNH motif has also been identified in nonspecific nucleases such the E. coli colicins (e.g. ColE9 and ColE7), EndA from S. pneumoniae, NucA from Anabaena and CAD (Midon, Schafer et al. 2011). As well as having the HNH motif, several of these nucleases contain the signature DRGH motif and share structural homology with core elements forming the ββα-Me-finger active site motif. Mutational studies of residues in the HNH/DRGH motifs have confirmed their role in nucleic acid cleavage activity (Ku, Liu et al. 2002; Doudeva, Huang et al. 2006; Eastberg, Eklund et al. 2007; Huang and Yuan 2007). Furthermore, the DNA binding affinity and sequence preference for ColE7 could be effectively altered (Wang, Wright et al. 2009). Such detailed studies illustrate the potential in re-engineering nonspecific nucleases for targeted purposes.

Zinc-finger nucleases (ZFNs), generated by fusing Zinc-finger-based DNA-binding domains to an independent catalytic domain via a flexible linker (Kim, Cha et al. 1996; Smith, Berg et al. 1999; Smith, Bibikova et al. 2000), represent another type of engineered nuclease commonly used to stimulate gene targeting. The archetypal ZFNs are based on the catalytic domain of the Type IIS restriction enzyme FokI and have been successfully used to induce gene correction, gene insertion, and gene deletion. Zinc Finger-based DNA binding domains are made of strings of 3 or 4 individual Zinc Fingers, each recognizing a DNA triplet (Pabo, Peisach et al. 2001). In theory, one of the major advantages of ZFNs is that they are easy to design, using combinatorial assembly of preexisting Zinc Fingers with known recognition patterns (Choo and Klug 1994; Choo and Klug 1994; Kim, Lee et al. 2009). However, close examination of high resolution structures shows that there are actually cross-talks between units (Elrod-Erickson, Rould et al. 1996), and several methods have been used to assemble ZF proteins by choosing individual Zinc Fingers in a context dependant manner (Greisman and Pabo 1997; Isalan and Choo 2001; Maeder, Thibodeau-Beganny et al. 2008; Ramirez, Foley et al. 2008) to achieve better success rates and reagents of better quality.

Recently, a new class of chimeric nuclease using a FokI catalytic domain has been described (Christian, Cermak et al. 2010; Li, Huang et al. 2011). The DNA binding domain of these nucleases is derived from Transcription Activator Like Effectors (TALE), a family of proteins used in the infection process by plant pathogens of the Xanthomonas genus. In these DNA binding domains, sequence specificity is driven by a series of 33-35 amino acids repeats, differing essentially by two positions (Boch, Scholze et al. 2009; Moscou and Bogdanove 2009). Each base pair in the DNA target is contacted by a single repeat, with the specificity resulting from the two variant amino acids of the repeat (the so-called repeat variable dipeptide, RVD). The apparent modularity of these DNA binding domains has been confirmed to a certain extent by modular assembly of designed TALE-derived protein with new specificities (Boch, Scholze et al. 2009; Moscou and Bogdanove 2009). However, one cannot yet rule out a certain level of context dependence of individual repeat/base recognition patterns, as was observed for Zinc Finger proteins (see above). Furthermore, it has been shown that natural TAL effectors can dimerize (Gurlebeck, Szurek et al. 2005) and how this would affect a “dimerization-based” TALE-derived nuclease is currently unknown.

The functional layout of a FokI-based TALE-nuclease (TALEN) is essentially that of a ZFN, with the Zinc-finger DNA binding domain being replaced by the TALE domain (Christian, Cermak et al. 2010; Li, Huang et al. 2011). As such, DNA cleavage by a TALEN requires two DNA recognition regions flanking an unspecific central region. This central “spacer” DNA region is essential to promote catalysis by the dimerizing FokI catalytic domain, and extensive effort has been placed into optimizing the distance between the DNA binding sites (Christian, Cermak et al. 2010; Miller, Tan et al. 2011). The length of the spacer has been varied from 14 to 30 base pairs, with efficiency in DNA cleavage being interdependent with spacer length as well as TALE scaffold construction (i.e. the nature of the fusion construct used). It is still unknown whether differences in the repeat region (i.e. RVD type and number used) have an impact on the DNA “spacer” requirements or on the efficiency of DNA cleavage by TALENs. Nevertheless, TALE-nucleases have been shown to be active to various extents in cell-based assays in yeast, mammalian cells and plants (Christian, Cermak et al. 2010; Li, Huang et al. 2011; Mahfouz, Li et al. 2011; Miller, Tan et al. 2011).

The inventors have developed a new type of TALEN that can be engineered to specifically recognize and process target DNA efficiently. These novel “compact TALENs” (cTALENs) do not require dimerization for DNA processing activity, thereby alleviating the need for “dual” target sites with intervening DNA “spacers”. Furthermore, the invention allows for generating several distinct types of enzymes that can enhance separate DNA repair pathways (HR vs. NHEJ).

BRIEF SUMMARY OF THE INVENTION

The present invention relates to a method to generate compact Transcription Activator-Like Effector Nucleases (TALENs) composed of a single polypeptide chain that do not require dimerization to target a specific single double-stranded DNA target sequence of interest and process DNA nearby said single double-stranded DNA target sequence of interest. The present invention also concerns the creation of functional single polypeptide fusion proteins for simple and efficient vectorization. In another aspect, the present invention relates to compact TALENs comprising at least an enhancer domain wherein said enhancer domain enhances the DNA processing efficiency of said compact TALENS nearby a single double-stranded DNA target sequence of interest. The present invention also relates to compact TALENS, vectors, compositions and kits used to implement the method. The present invention also relates to methods for use of said compact TALENs according to the invention for various applications ranging from targeted DNA cleavage to targeted gene regulation. The methods according to the present invention can be used in various fields ranging from the creation of transgenic organisms to treatment of genetic diseases.

BRIEF DESCRIPTION OF THE FIGURES

In addition to the preceding features, the invention further comprises other features which will emerge from the description which follows, as well as to the appended drawings. A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following Figures in conjunction with the detailed description below.

FIG. 1: Endonuclease-induced gene targeting approaches. Upon cleavage, DNA repair mechanisms may result in one of several outcomes. (A) When a double-strand break is targeted between two direct repeats, HR can result in the deletion of one repeat together with the intervening sequence. Gene insertion (B) or correction (C) can be achieved by the introduction of a DNA repair matrix containing sequences homologous to the endogenous sequence surrounding the DNA break. Mutations can be corrected either at or distal to the break, with the frequency of correction decreasing with increasing distance. (D) The misrepair of DNA ends by error-prone NHEJ can result in insertions or deletions of various sizes, leading to gene inactivation.

FIG. 2: Sequences of target DNA recognized by I-CreI and I-TevI. C1234 (SEQ ID NO: 3) represents the partially symmetric natural DNA sequence recognized and cleaved by the wild-type I-CreI meganuclease. C1221 (SEQ ID NO: 2) represents an artificial palindromic DNA sequence, derived from C1234 (SEQ ID NO: 3), also recognized and cleaved by I-CreI (SEQ ID NO: 1). Nucleotides are numbered outward (−/+) from the center of the target. DNA cleavage occurs on either side of the underlined sequence to generate 4-nucleotide 3′ overhanging ends. For I-CreI-based meganucleases, the nature of the nucleotides at positions −2 to +2 can potentially interfere with the cleavage activity of the protein. Tev (SEQ ID NO: 105) represents the asymmetric DNA sequence recognized and cleaved by the wild-type I-TevI meganuclease. Nucleotide numbering is relative to the intron-insertion site of the natural target sequence. Cleavage by I-TevI occurs on either side of the underlined sequence to generate 2-nucleotide 3′ overhanging ends.

FIG. 3: Sequences of the target DNAs recognized by TALEN and compact TALEN constructs. Target DNAs for the engineered compact TALENS cTN-Avr and cTN-Pth are based on the naturally occurring asymmetric sequences AvrBs3 (19 bp) [in bT1-Avr (SEQ ID NO: 136) and bT2-Avr (SEQ ID NO: 137) baseline protein scaffolds] and PthXo1 (25 bp) [in bT1-Pth (SEQ ID NO: 138) and bT2-Pth (SEQ ID NO: 139) baseline protein scaffolds], respectively. For each sequence, nucleotides are numbered outward (−/+) from the anchoring T (position −1). Sequences shown are directly contacted by the protein to provide target specificity. Wild-type Repeat Variable Dipeptides (RVDs) correspond to the dipeptides found in the repeats of the naturally occurring effector proteins targeted to each sequence. Cipher RVDs are based on the subset of dipeptide/nucleotide pairs listed. Artificial RVDs are derived by direct readout of the underlying DNA sequence using the cipher RVD code (SEQ ID NO: 245 to 249).

FIG. 4: Schematic of meganuclease fusion configurations. Fusion constructs are optimized to address or overcome distinct problems. (A) The addition of two catalytic domains to an active meganuclease can not only enhance cleavage activity (e.g. three chances to effect DNA cleavage per binding event) but can also promote sequence alterations by error-prone NHEJ since small sections of DNA are excised for each pair of cleavage events. (B) When specificity reengineering precludes maintaining cleavage activity of the meganuclease, the attached catalytic domains provide the necessary strand cleavage function. (C) and (D) represent instances of (A) and (B), respectively, when only one catalytic domain is tolerated per fusion protein (e.g. either as an N- or C-terminal fusion or in the context of a single-chain molecule). In all cases, the catalytic domain envisioned can be either a cleavase (ability to cleave both strands of the DNA) or a nickase (cleavage of only a single DNA strand) depending on the application. Fusion junctions (N- vs. C-terminal) and linker designs can vary with the application. Components of the fusion proteins are listed in the legend.

FIG. 5: Schematic of cTALEN configurations. Compact TALENs are designed to alleviate the need for multiple independent protein moieties when targeting a DNA cleavage event. Importantly, the requisite “spacer” region and dual target sites essential for the function of current classical TALENs are unnecessary. In addition, since the catalytic domain does not require specific DNA contacts, there are no restrictions on regions surrounding the core TALE DNA binding domain. (A) N-terminal fusion construct to promote HR via a standard (cleavase domain) or conservative (nickase domain) repair pathway. (B) C-terminal fusion construct with properties as in (A). (C) The attachment of two catalytic domains to both ends of the TALE allows for dual cleavage with enhancement in NHEJ. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application. Components of the fusion proteins are listed in the legend.

FIG. 6: Schematic of enhanced cTALEN configurations. Compact TALENs can be enhanced through the addition of a domain to promote existing or alternate activities. As each end of the TALE DNA binding domain is amenable to fusion, the order (N- v.s C-terminal) of addition of the catalytic and enhancer domains can vary with the application. (A) A standard cTALEN with a C-terminal enhancer domain. (B) The enhancer domain is fused to the cTALEN via the N-terminus of the catalytic domain. Such a configuration can be used to assist and/or anchor the catalytic domain near the DNA to increase cleavage activity. (C) The enhancer domain is sandwiched between the catalytic domain and TALE DNA binding domain. The enhancer domain can promote communication between the flanking domains (i.e. to assist in catalysis and/or DNA binding) or can be used to overcome the requisite T nucleotide at position −1 of all TALE-based targets. (D) The enhancer domain is used to functionally replace the natural TALE protein N-terminal region. (E) The enhancer domain is used to functionally replace the natural TALE protein C-terminal region. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application. Components of the fusion proteins are listed in the legend.

FIG. 7: Schematic of trans cTALEN configurations. Compact TALENs can be combined with auxiliary enhancer domains to promote alternate activities. Auxiliary domains provide an additional function that is not essential to the cTALEN activity. (A) A standard cTALEN with an N-terminal nickase catalytic domain becomes a “cleavase” via the separate addition of the auxiliary domain. (B) In some instances, the need to target the specificity of the auxiliary domain is necessary. Such a configuration can achieved via a TALE fusion and can be used to assist and/or anchor the auxiliary domain near the DNA to increase activity of the cTALEN. (C) The targeted auxiliary domain is provided either before or after the cTALEN to perform an independent task. Communication between the fusion proteins is not necessary. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application. Components of the fusion proteins are listed in the legend.

FIG. 8: Schematic of DNA cleavage, in vivo re-ligation and other repair pathways. In cells, cleavage by peptidic rare-cutting endonucleases usually results in a DNA double strand break (DSB) with cohesive ends. For example, meganucleases from the LAGLIDADG family, such as I-SceI and I-CreI, produce DSBs with 3′ overhangs. These cohesive ends can be re-ligated in vivo by NHEJ, resulting in seamless repair, and in the restoration of a cleavable target sequence, which can in turn be processed again by the same endonuclease. Thus, a series of futile cycles of cleavage and re-ligation events can take place. Imprecise NHEJ or homologous recombination can alter or remove the cleavage site, resulting in cycle exit; this can also apply to compact TALENs and enhanced compact TALENs according to the present invention (A). Two other ways can also stop the process: (i) Chromosome loss can occur as the consequence of failure to repair the DSB; (ii) a loss of nuclease (degradation, dilution, cell division, etc. . . . ). B-E: Consequences of cleavage of additional phosphodiester bonds. The addition of a single nickase activity (B) or of two nickase activities affecting the same strand (C) would result in a single strand gap, and suppress the cohesive ends, which could in turn affect the spectrum of events. Addition of two nickase activities affecting opposite strands (D) or of a new cleavase activity generating a second DSB (E) would result in a double strand gap; as a consequence, perfect re-ligation is no longer possible, and one or several alternative repair outcomes could be stimulated. The current figure makes no assumption regarding the relative frequencies of these alternative outcomes (imprecise NHEJ, homologous recombination, others . . . ). Solid triangles represent hydrolysis of phosphodiester bonds.

FIG. 9: Activity of TALE-AvrBs3::TevI in yeast (37° C.). The negative control consists in a TALEN without any RVDs. n.d. indicates no detectable activity, +indicates an activity over 0.3 in yeast assay and +++indicates an activity over 0.7 in yeast assay (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 10: Activity of TALE-AvrBs3::TevI in mammalian cells. (Extrachromosomic assay in CHO-K1). pCLS8993 (SEQ ID NO: 194) is represented by a black bar and pCLS8994 (SEQ ID NO: 195) is represented by a dark grey bar. Negative control (empty vector) by a white bar and positive control (I-SceI meganuclease) by a light grey bar. Data are normalized relative to the positive control.

FIG. 11: Activity of TALE-AvrBs3::NucA in yeast (37° C.). The negative control is a target lacking a recognition site (neg. ctrl.: SEQ ID NO: 228). Compact is a target having only one recognition site (SEQ ID NO: 224). n.d. indicates no detectable activity, +indicates an activity over 0.3 in yeast assay at 37° C.; ++, activity over 0.5 in yeast assay at 37° C. and +++activity over 0.7 in yeast assay at 37° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 12: Activity of TALE-AvrBs3::ColE7 in yeast (37° C.). The negative control is a target lacking a recognition site (neg. ctrl.: SEQ ID NO: 228). Compact is a target having only one recognition site (SEQ ID NO: 224). n.d. indicates no detectable activity, +indicates an activity over 0.3 in yeast assay at 37° C.; ++, activity over 0.5 in yeast assay at 37° C. and +++activity over 0.7 in yeast assay at 37° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 13: Schematic and details of a TALE::CreI prototypical compact TALEN. This class of compact TALEN targets a bipartite recognition sequence comprised of the TALE DNA binding site proximal to a meganuclease target site. The engineered TCRB02-A meganuclease site (SEQ ID NO:456) is shown along with details of the RVDs (TCRB2A1, SEQ ID NO:460, TCRB2A2, SEQ ID NO:461 TCRB2A3, SEQ ID NO:462) and DNA sequences recognized by the TALE moiety (TCRB2A1 target SEQ ID NO:457, TCRB2A2 target SEQ ID NO:458 TCRB2A3 target SEQ ID NO:459). A region of the T cell receptor B gene is presented (SEQ ID NO: 463), highlighting the endogenous layout of the TALE: :CreI-based compact TALEN hybrid target site.

FIG. 14: Activity of TALE::scTB2aD01-based constructs in yeast (30° C.). The layouts of the various hybrid targets are shown (TCRB02.1; SEQ ID NO: 464; TCRB02Tsp07; SEQ ID NO: 465; TCRB02Tsp12; SEQ ID NO: 466; TCRB02sp16; SEQ ID NO: 467), starting (5′) with the region recognized by the TALE DNA binding domain in uppercase, the unspecific spacer region in lowercase and the meganuclease target site in underlined uppercase characters. Activity in yeast is illustrated for select representative constructs. n.d. indicates no detectable activity, +indicates an activity over 0.3 in yeast assay at 30° C.; ++, activity over 0.5 in yeast assay at 30° C. and +++activity over 0.7 in yeast assay at 30° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 15: Western blot of TALE::scTB2aD01-based constructs. Constructs were expressed in HEK293 cells and total protein extracts were prepared 48 hours post-transfection. Protein was detected using a polyclonal anti-1-CreI antibody.

FIG. 16: Toxicity of TALE::scTB2aD01-based constructs in CHOK1 cells. Cytotoxicty is based on detectable levels of GFP expressed in living cells, on day 1 vs day 6, relative to a standard control (transfection of empty plasmid).

FIG. 17: NHEJ activity of TALE::scTB2aD01-based constructs in HEK293 cells. A post-transfection PCR-based analysis of genomic DNA is used to assess activity in vivo. Cleavage of mismatched DNA sequences by T7 endonuclease is indicative of NHEJ events resulting from the activity of the cTALEN or meganuclease at the targeted locus.

FIG. 18: Activity of TevI::TALE-AvrBs3+/−-TALE-RagT2-R::TevI in yeast (37° C.). The negative control is a target lacking a recognition site (neg. ctrl.: SEQ ID NO: 228). n.d. indicates no detectable activity, +indicates an activity over 0.3 in yeast assay at 37° C.; ++, activity over 0.5 in yeast assay at 37° C. and +++activity over 0.7 in yeast assay at 37° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 19: Activity of TALE::SnaseSTAAU in yeast (37° C.). The negative control is a target lacking recognition sites. Compact is a target having only one recognition site (SEQ ID NO: 224). n.d. indicates no detectable activity at 37° C., +/−indicated an activity above 0.3 in yeast assay at 37° C.; +indicated an activity over 0.3 in yeast assay at 37° C.; ++indicated an activity over 0.5 in yeast assay at 37° C.; +++indicated an activity over 0.75 in yeast assay at 37° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 20: Activity of TALENColE7 with various polypeptide linker in yeast (37° C.). Compact is a target having only one recognition site (SEQ ID NO: 224). n.d. indicates no detectable activity at 37° C., +indicated an activity over 0.3 in yeast assay at 37° C.; ++indicated an activity over 0.5 in yeast assay at 37° C.; +++indicated an activity over 0.75 in yeast assay at 37° C. (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

FIG. 21: List of AvrBs3 targets with various spacer lengths (SEQ ID NO: 157 to 192).

FIG. 22: List of AvrBs3 targets with various spacer lengths (SEQ ID NO: 157 to 192) including a target with only one recognition site (compact, SEQ ID NO: 224) and a negative control target (neg. ctrl., SEQ ID NO: 228) consisting in a target without any recognition site.

FIG. 23: List of hybrid RagT2-R/AvrBs3 targets with various spacer lengths (SEQ ID NO: 315 to 350).

DETAILED DESCRIPTION OF THE INVENTION

Unless specifically defined herein, all technical and scientific terms used have the same meaning as commonly understood by a skilled artisan in the fields of gene therapy, biochemistry, genetics, and molecular biology.

All methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, with suitable methods and materials being described herein. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will prevail. Further, the materials, methods, and examples are illustrative only and are not intended to be limiting, unless otherwise specified.

The practice of the present invention will employ, unless otherwise indicated, conventional techniques of cell biology, cell culture, molecular biology, transgenic biology, microbiology, recombinant DNA, and immunology, which are within the skill of the art. Such techniques are explained fully in the literature. See, for example, Current Protocols in Molecular Biology (Frederick M. AUSUBEL, 2000, Wiley and son Inc, Library of Congress, USA); Molecular Cloning: A Laboratory Manual, Third Edition, (Sambrook et al, 2001, Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press); Oligonucleotide Synthesis (M. J. Gait ed., 1984); Mullis et al. U.S. Pat. No. 4,683,195; Nucleic Acid Hybridization (B. D. Harries & S. J. Higgins eds. 1984); Transcription And Translation (B. D. Hames & S. J. Higgins eds. 1984); Culture Of Animal Cells (R. I. Freshney, Alan R. Liss, Inc., 1987); Immobilized Cells And Enzymes (IRL Press, 1986); B. Perbal, A Practical Guide To Molecular Cloning (1984); the series, Methods In ENZYMOLOGY (J. Abelson and M. Simon, eds.-in-chief, Academic Press, Inc., New York), specifically, Vols. 154 and 155 (Wu et al. eds.) and Vol. 185, “Gene Expression Technology” (D. Goeddel, ed.); Gene Transfer Vectors For Mammalian Cells (J. H. Miller and M. P. Calos eds., 1987, Cold Spring Harbor Laboratory); Immunochemical Methods In Cell And Molecular Biology (Mayer and Walker, eds., Academic Press, London, 1987); Handbook Of Experimental Immunology, Volumes I-IV (D. M. Weir and C. C. Blackwell, eds., 1986); and Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986).

In a first aspect, the present invention relates to a method to generate compact Transcription Activator-Like Effector Nucleases (cTALENs) composed of a single polypeptide chain that do not require dimerization to target a specific single double-stranded DNA target sequence of interest and process DNA nearby said single double-stranded DNA target sequence of interest.

According to a first aspect of the present invention is a method to generate compact Transcription Activator-Like Effector Nucleases (cTALENs) comprising the steps of:

-   -   (i) Engineering a core TALE scaffold (a) comprising different         sets of Repeat Variable Dipeptide regions (RVDs) to change DNA         binding specificity and target a specific single double-stranded         DNA target sequence of interest, (b) onto which a selection of         catalytic domains can be attached to effect DNA processing;     -   (ii) Determining or engineering at least one catalytic domain         wherein said catalytic domain is capable of processing DNA         nearby said single double-stranded DNA target sequence of         interest when fused to said engineered core TALE scaffold from         (i);     -   (iii) Optionally determining or engineering a peptidic linker to         fuse said catalytic domain from (ii) to said engineered core         TALE scaffold from (i);         thereby obtaining a compact TALEN entity composed of a single         polypeptide chain that does not require dimerization to target a         specific single double-stranded DNA target sequence of interest         and process DNA nearby said single double-stranded DNA target         sequence of interest. In other words, the compact TALEN         according to the present invention is an active entity unit         able, by itself, to target only one specific single         double-stranded DNA target sequence of interest through one DNA         binding domain and to process DNA nearby said single         double-stranded DNA target sequence of interest.

In another embodiment, is a method for targeting and processing a double-stranded DNA, comprising:

-   -   (a) Selecting one DNA target sequence of interest on one strand         of a double-stranded DNA;     -   (b) Providing a unique compact TALEN monomer comprising:         -   (i) One core TALE scaffold comprising Repeat Variable             Dipeptide regions (RVDs) having DNA binding specificity onto             said DNA target sequence of interest;         -   (ii) At least one catalytic domain wherein said catalytic             domain is capable of processing DNA a few base pairs away             from said DNA target sequence of interest when fused to the             C and/or N terminal of said core TALE scaffold from (i);         -   (iii) Optionally one peptidic linker to fuse said catalytic             domain from (ii) to said core TALE scaffold from (i) when             needed;     -   wherein said compact TALEN monomer is assembled to bind and         process said double stranded DNA without requiring dimerization;     -   (c) Contacting said double-stranded DNA with said unique monomer         such that the double-stranded is processed a few base pairs away         in 3′ and/or 5′ direction(s) from said one strand target         sequence.

In another embodiment, said engineered core TALE scaffold according to the present invention comprises an additional N-terminal domain resulting in an engineered core TALE scaffold sequentially comprising a N-terminal domain and different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest, onto which a selection of catalytic domains can be attached to effect DNA processing.

In another embodiment, said engineered core TALE scaffold according to the present invention comprises an additional C-terminal domain resulting in an engineered core TALE scaffold sequentially comprising different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest and a C-terminal domain, onto which a selection of catalytic domains can be attached to effect DNA processing.

In another embodiment, said engineered core TALE-scaffold according to the present invention comprises additional N-terminus and a C-terminal domains resulting in an engineered core TALE scaffold sequentially comprising a N-terminal domain, different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest and a C-terminal domain, onto which a selection of catalytic domains can be attached to effect DNA processing. In another embodiment, said engineered core TALE-scaffold according to the present invention comprises the protein sequences selected from the group consisting of ST1 (SEQ ID NO: 134) and ST2 (SEQ ID NO: 135). In another embodiment, said engineered TALE-scaffold comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 134 and SEQ ID NO: 135.

In another embodiment, said engineered core TALE-scaffold according to the present invention comprises the protein sequences selected from the group consisting of bT1-Avr (SEQ ID NO: 136), bT2-Avr (SEQ ID NO: 137), bT1-Pth (SEQ ID NO: 138) and bT2-Pth (SEQ ID NO: 139). In another embodiment, said engineered TALE-scaffold comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 136 to SEQ ID NO: 139.

In a preferred embodiment according to the method of the present invention, said additional N-terminus and C-terminal domains of engineered core TALE scaffold are derived from natural TALE. In a more preferred embodiment said additional N-terminus and C-terminal domains of engineered core TALE scaffold are derived from natural TALE like AvrBs3, PthXo1, AvrHah1, PthA, Tal1c as non-limiting examples. In another more preferred embodiment, said additional N-terminus and/or said C-terminal domains are truncated forms of respective N-terminus and/or said C-terminal domains of natural TALE like AvrBs3, PthXo1, AvrHah1, PthA, Tal1c as non-limiting examples from which they are derived. In a more preferred embodiment, said additional N-terminus and C-terminal domains sequences of engineered core TALE scaffold are selected from the group consisting of ST1 SEQ ID NO: 134 and ST2 SEQ ID NO: 135 as respectively exemplified in baseline protein scaffolds bT1-Avr (SEQ ID NO: 136) or bT1-Pth (SEQ ID NO: 138) and bT2-Avr (SEQ ID NO: 137) or bT2-Pth (SEQ ID NO: 139).

In another embodiment, each RVD of said core scaffold is made of 30 to 42 amino acids, more preferably 33 or 34 wherein two critical amino acids located at positions 12 and 13 mediates the recognition of one nucleotide of said nucleic acid target sequence; equivalent two critical amino acids can be located at positions other than 12 and 13 specially in RVDs taller than 33 or 34 amino acids long. Preferably, RVDs associated with recognition of the different nucleotides are HD for recognizing C, NG for recognizing T, NI for recognizing A, NN for recognizing G or A, NS for recognizing A, C, G or T, HG for recognizing T, IG for recognizing T, NK for recognizing G, HA for recognizing C, ND for recognizing C, HI for recognizing C, HN for recognizing G, NA for recognizing G, SN for recognizing G or A and YG for recognizing T, TL for recognizing A, VT for recognizing A or G and SW for recognizing A. More preferably, RVDs associated with recognition of the nucleotides C, T, A, G/A and G respectively are selected from the group consisting of NN or NK for recognizing G, HD for recognizing C, NG for recognizing T and NI for recognizing A, TL for recognizing A, VT for recognizing A or G and SW for recognizing A. In another embodiment, RVDS associated with recognition of the nucleotide C are selected from the group consisting of N* and RVDS associated with recognition of the nucleotide T are selected from the group consisting of N* and H*, where * denotes a gap in the repeat sequence that corresponds to a lack of amino acid residue at the second position of the RVD. In another embodiment, critical amino acids 12 and 13 can be mutated towards other amino acid residues in order to modulate their specificity towards nucleotides A, T, C and G and in particular to enhance this specificity. By other amino acid residues is intended any of the twenty natural amino acid residues or unnatural amino acids derivatives.

In another embodiment, said core scaffold of the present invention comprises between 8 and 30 RVDs. More preferably, said core scaffold of the present invention comprises between 8 and 20 RVDs; again more preferably 15 RVDs.

In another embodiment, said core scaffold comprises an additional single truncated RVD made of 20 amino acids located at the C-terminus of said set of RVDs, i.e. an additional C-terminal half-RVD. In this case, said core scaffold of the present invention comprises between 8.5 and 30.5 RVDs, “0.5” referring to previously mentioned half-RVD (or terminal RVD, or half-repeat). More preferably, said core scaffold of the present invention comprises between 8.5 and 20.5 RVDs, again more preferably, 15.5 RVDs. In a preferred embodiment, said half-RVD is in a core scaffold context which allows a lack of specificity of said half-RVD toward nucleotides A, C, G, T. In a more preferred embodiment, said half-RVD is absent.

In another embodiment, said core scaffold of the present invention comprises RVDs of different origins. In a preferred embodiment, said core scaffold comprises RVDs originating from different naturally occurring TAL effectors. In another preferred embodiment, internal structure of some RVDs of the core scaffold of the present invention are constituted by structures or sequences originated from different naturally occurring TAL effectors. In another embodiment, said core scaffold of the present invention comprises RVDs-like domains. RVDs-like domains have a sequence different from naturally occurring RVDs but have the same function and/or global structure within said core scaffold of the present invention.

In another embodiment, said additional N-terminal domain of said engineered core TALE scaffold is an enhancer domain. In another embodiment, said enhancer domain is selected from the group consisting of Puf RNA binding protein or Ankyrin super-family, as non-limiting examples. In another embodiment, said enhancer domain sequence is selected from the group consisting of protein domains of SEQ ID NO: 4 and SEQ ID NO: 5, as non-limiting examples listed in Table 1, a functional mutant, a variant or a derivative thereof.

In another embodiment, said additional C-terminal domain of said engineered core TALE scaffold is an enhancer domain. In another embodiment, said enhancer domain is selected from the group consisting of hydrolase/transferase of Pseudomonas Aeuriginosa family, the polymerase domain from the Mycobacterium tuberculosis Ligase D family, the initiation factor elF2 from Pyrococcus family, the translation initiation factor Aif2 family, as non-limiting examples. In another embodiment, said enhancer domain sequence is selected from the group consisting of protein domains of SEQ ID NO: 6 to SEQ ID NO: 9, as non-limiting examples listed in Table 1, a functional mutant, a variant or a derivative thereof.

TABLE 1 List of enhancer domains for engineered core TALE scaffold. SEQ GENBANK/SWISS- ID PROT ID NAME NO FASTA SEQUENCE gi|262368139|pdb| fem-3 4 >gi|262368139|pdb|3K5Q|A Chain A, Crystal Structure Of Fbf-2FBE    3K5Q| COMPLEX SNNVLPTWSLDSNGEMRSRLSLSEVLDSGDLMKFAVDKTGCQFLEKAVKGSLTSYQKFQLFEQV IGRKDDFLKLSTNIFGNYLVQSVIGISLATNDDGYTKRQEKLKNFISSQMTDMCLDKFACRVIQ SSLQNMDLSLACKLVQALPRDARLIAICVDQNANHVIQKVVAVIPLKNWEFIVDFVATPEHLRQ ICSDKYGCRVVQTIIEKLTADSMNVDLTSAAQNLRERALQRLMTSVTNRCQELATNEYANYIIQ HIVSNDDLAVYRECIIEKCLMRNLLSLSQEKFASHVVEKAFLHAPLELLAEMMDEIFDGYIPHP DTGKDALDIMMFHQFGNYVVQCMLTICCDAVSGRRQTKEGGYDHAISFQDWLKKLHSRVTKERH RLSRFSSGKKMIETLANLRSTHPIYELQ gi|308387836|pdb| aRep 5 >gi|308387836|pdb|3LTJ|A Chain A, Structure Of A New Family Of 3LTJ| Artificial Alpha Helicoidal Repeat Proteins (Alpha-Rep) Based On Thermostable Heat-Like Repeats MRGSHHHHHHTDPEKVEMYIKNLQDDSYYVRRAAAYALGKIGDERAVEPLIKALKDEDAWVRRA AADALGQIGDERAVEPLIKALKDEDGWVRQSAAVALGQIGDERAVEPLIKALKDEDWFVRIAAA FALGEIGDERAVEPLIKALKDEDGWVRQSAADALGEIGGERVRAAMEKLAETGTGFARKVAVNY LETHKSLIS gi|109157579|pdb| Pseudomonas 6 >gi|109157579|pdb|2FAO|A Chain A, Crystal Structure Of 2FAO| Aeruginosa Ligd Pseudomonas Aeruginosa Ligd Polymerase Domain Polymerase MGARKASAGASRAATAGVRISHPQRLIDPSIQASKLELAEFHARYADLLLRDLRERPVSLVRGP Domain DGIGGELFFQKHAARLKIPGIVQLDPALDPGHPPLLQIRSAEALVGAVQMGSIEFHTWNASLAN LERPDRFVLDLDPDPALPWKRMLEATQLSLTLLDELGLRAFLKTSGGKGMHLLVPLERRHGWDE VKDFAQAISQHLARLMPERFSAVSGPRNRVGKIFVDYLRNSRGASTVAAYSVRAREGLPVSVPV FREELDSLQGANQWNLRSLPQRLDELAGDDPWADYAGTRQRISAAMRRQLGRG 2R9L_A GI: Mycobacterium 7 Polymerase Domain From Mycobacterium Tuberculosis Ligase D In 164519498 Tuberculosis Complex With Dna:Accession: 2R9L_A GI: 164519498 Ligase D >gi|164519498|pdb|2R9L|A Chain A, Polymerase Domain From Mycobacterium Tuberculosis Ligase D In Complex With Dna GSHMGSASEQRVTLTNADKVLYPATGTTKSDIFDYYAGVAEVMLGHIAGRPATRKRWPNGVDQP AFFEKQLALSAPPWLSRATVAHRSGTTTYPIIDSATGLAWIAQQAALEVHVPQWRFVAEPGSGE LNPGPATRLVFDLDPGEGVMMAQLAEVARAVRDLLADIGLVTFPVTSGSKGLHLYTPLDEPVSS RGATVLAKRVAQRLEQAMPALVTSTMTKSLRAGKVFVDWSQNSGSKTTIAPYSLRGRTHPTVAA PRTWAELDDPALRQLSYDEVLTRIARDGDLLERLDADAPVADRLTRY 1KJZ_A Large Gamma 8 Structure Of The Large Gamma Subunit Of Initiation Factor Eif2 GI:20664108 Subunit Of From Pyrococcus Abyssi-G235d Mutant:1KJZ_A GI:20664108, Initiation >gi|20664108|pdb|1KJZ|A Chain A, Structure Of The Large Gamma Factor Eif2 Subunit Of Initiation Factor Eif2 From Pyrococcus Abyssi-G235d From Pyrococcus Mutant Abyssi GEKRKSRQAEVNIGMVGHVDHGKTTLTKALTGVWTDTHSEELRRGITIKIGFADAEIRRCPNCG RYSTSPVCPYCGHETEFVRRVSFIDAPGHEALMTTMLAGASLMDGAILVIAANEPCPRPQTREH LMALQIIGQKNIIIAQNKIELVDKEKALENYRQIKEFIEGTVAENAPIIPISALHGANIDVLVK AIEDFIPTPKRDPNKPPKMLVLRSFDVNKPGTPPEKLVGGVLDGSIVQGKLKVGDEIEIRPGVP YEEHGRIKYEPITTEIVSLQAGGQFVEEAYPGGLVGVGTKLDPYLTKGDLMAGNVVGKPGKLPP VWDSLRLEVHLLERVVGTEQELKVEPIKRKEVLLLNVGTARTMGLVTGLGKDEIEVKLQIPVCA EPGDRVAISRQIGSRWRLIGYGIIKE 2D74_A Translation 9 Crystal Structure Of Translation Initiation Factor Aif2betagamma GI:112490420 Initiation Heterodimer:2D74_A GI:112490420, Factor >gi|112490420|pdb|2D74|A Chain A, Crystal Structure Of Aif2betagamma Translation Initiation Factor Aif2betagamma Heterodimer MGEKRKTRQAEVNIGMVGHVDHGKTTLTKALTGVWTDTHSEELRRGITIKIGFADAEIRRCSNC GRYSTSPICPYCGHETEFIRRVSFIDSPGHEALMTTMLAGASLMDGAILVIAANEPCPRPQTRE HLMALQIIGQKNIIIAQNKIELVDKEKALENYRQIKEFIKGTVAENAPIIPISALHGANIDVLV KAIEEFIPTPKRDSNKPPKMLVLRSFDVNKPGTPPEKLVGGVLDGSIVQGKLKVGDEIEIRPGV PYEEHGRIKYEPITTEIVSLQAGGQFVEEAYPGGLVGIGTKLDPYLTKGDLMAGNVVGKPGKLP PVWTDLRLEVHLLERVVGTEQELNVEPIKRKEVLLLNVGTARTMGLVTALGKDEIELKLQIPVC AEPGERVAISRQIGSRWRLIGYGIIKELEHHHHHH

In another preferred embodiment according to the method of the present invention, the catalytic domain that is capable of processing DNA nearby the single double-stranded DNA target sequence of interest, when fused to said engineered core TALE scaffold according to the method of the present invention, is fused to the N-terminus part of said core TALE scaffold. In another preferred embodiment, said catalytic domain is fused to the C-terminus part of said core TALE scaffold. In another preferred embodiment two catalytic domains are fused to both N-terminus part of said core TALE scaffold and C-terminus part of said core TALE scaffold. In a more preferred embodiment, said catalytic domain has an enzymatic activity selected from the group consisting of nuclease activity, polymerase activity, kinase activity, phosphatase activity, methylase activity, topoisomerase activity, integrase activity, transposase activity or ligase activity. In another preferred embodiment, the catalytic domain fused to the core TALE scaffold of the present invention can be a transcription activator or repressor (i.e. a transcription regulator), or a protein that interacts with or modifies other proteins such as histones. Non-limiting examples of DNA processing activities of said compact TALEN of the present invention include, for example, creating or modifying epigenetic regulatory elements, making site-specific insertions, deletions, or repairs in DNA, controlling gene expression, and modifying chromatin structure.

In another more preferred embodiment, said catalytic domain has an endonuclease activity. In another more preferred embodiment, said catalytic domain has cleavage activity on said double-stranded DNA according to the method of the present invention. In another more preferred embodiment, said catalytic domain has a nickase activity on said double-stranded DNA according to the method of the present invention. In another more preferred embodiment, said catalytic domain is selected from the group consisting of proteins MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative thereof. In another preferred embodiment according to the method of the present invention, said catalytic domain is I-TevI (SEQ ID NO: 20), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain I-TevI (SEQ ID NO: 20), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 420-432.

In another preferred embodiment, said catalytic domain is ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 435-438.

In another preferred embodiment, said catalytic domain is NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 433-434.

In another preferred embodiment, said catalytic domain is I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 439-441 and SEQ ID NO: 444-446.

In another embodiment, said catalytic domain is a restriction enzyme such as MmeI, R-HinPII, R.MspI, R.MvaI, Nb.BsrDI, BsrDI A, Nt.BspD6I, ss.BspD6I, R.PleI, MlyI and AlwI as non-limiting examples listed in table 2. In another more preferred embodiment, said catalytic domain has an exonuclease activity.

In another more preferred embodiment, any combinations of two catalytic domains selected from the group consisting of proteins MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative of these protein domains thereof, can be fused to both N-terminus part and C-terminus part of said core TALE scaffold, respectively. For example, I-HmuI catalytic domain can be fused to the N-terminus part of said core TALE scaffold and ColE7 catalytic domain can be fused to the C-terminus part of said core TALE scaffold. In another example, I-TevI catalytic domain can be fused to the N-terminus part of said core TALE scaffold and ColE7 catalytic domain can be fused to the C-terminus part of said core TALE scaffold. In another embodiment, according to the method of the present invention, said unique compact TALEN monomer comprises a combination of two catalytic domains respectively fused to the C-terminus part and to the N-terminus part of said core TALE scaffold selected from the group consisting of:

-   -   (i) A Nuc A domain (SEQ ID NO: 26) in N-terminus and a Nuc A         domain (SEQ ID NO: 26) in C-terminus;     -   (ii) A ColE7 domain (SEQ ID NO: 11) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus;     -   (iii) A TevI domain (SEQ ID NO: 20) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus;     -   (iv) A TevI domain (SEQ ID NO: 20) in N-terminus and a NucA         domain (SEQ ID NO: 26) in C-terminus;     -   (v) A ColE7 domain (SEQ ID NO: 11) in N-terminus and a NucA         domain (SEQ ID NO: 26) in C-terminus;     -   (vi) A NucA domain (SEQ ID NO: 26) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus.

In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 448 and 450.

In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a combination of two catalytic domains respectively fused to the C-terminus part and to the N-terminus part of said core TALE scaffold selected from the group consisting of:

-   -   (i) A TevI domain (SEQ ID NO: 20) in N-terminus and a FokI         domain (SEQ ID NO: 368) in C-terminus;     -   (ii) A TevI domain (SEQ ID NO: 20) in N-terminus and a TevI         domain (SEQ ID NO: 20) in C-terminus;     -   (iii) A scTrex2 domain (SEQ ID NO: 451) in N-terminus and a FokI         domain (SEQ ID NO: 368) in C-terminus.

In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 447-450 and SEQ ID NO: 452.

In the scope of the present invention, it can be envisioned to insert said catalytic domain between two parts of the engineered core TALE scaffold according to the invention, each part comprising one set of RVDs. In this last case, the number of RVDs for each part of the engineered core TALE scaffold can be the same or not. In other words, it can be envisioned to split said core TALE scaffold of the present invention to insert one catalytic domain between the resulting two parts of said engineered core TALE scaffold. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 453-455.

TABLE 2 List of catalytic/enhancer domains for compact TALENs or enhanced compact TALENs. GENBANK/ SWISS- SEQ ID PROT ID NAME NO FASTA SEQUENCE ACC85607.1 MmeI 10 >gi|186469979|gb|ACC85607.1| MmeI [Methylophilus methylotrophus] MALSWNEIRRKAIEFSKRWEDASDENSQAKPFLIDFFEVFGITNKRVATFEHAVKKFAKAHKEQSRGFVD LFWPGILLIEMKSRGKDLDKAYDQALDYFSGIAERDLPRYVLVCDFQRFRLTDLITKESVEFLLKDLYQN VRSFGFIAGYQTQVIKPQDPINIKAAERMGKLHDTLKLVGYEGHALELYLVRLLFCLFAEDTTIFEKSLF QEYIETKTLEDGSDLAHHINTLFYVLNTPEQKRLKNLDEHLAAFPYINGKLFEEPLPPAQFDKAMREALL DLCSLDWSRISPAIFGSLFQSIMDAKKRRNLGAHYTSEANILKLIKPLFLDELWVEFEKVKNNKNKLLAF HKKLRGLTFFDPACGCGNFLVITYRELRLLEIEVIRGLHRGGQQVLDIEHLIQINVDQFFGIEIEEFPAQ IAQVALWLTDHQMNMKISDEFGNYFARIPLKSTPHILNANALQIDWNDVLEAKKCCFILGNPPFVGKSKQ TPGQKADLLSVFGNLKSASDLDLVAAWYPKAAHYIQTNANIRCAFVSTNSITQGEQVSLLWPLLLSLGIK INFAHRTFSWTNEASGVAAVHCVIIGFGLKDSDEKIIYEYESINGEPLAIKAKNINPYLRDGVDVIACKR QQPISKLPSMRYGNKPTDDGNFLFTDEEKNQFITNEPSSEKYFRRFVGGDEFINNTSRWCLWLDGADISE IRAMPLVLARIKKVQEFRLKSSAKPTRQSASTPMKFFYISQPDTDYLLIPETSSENRQFIPIGFVDRNVI SSNATYHIPSAEPLIFGLLSSTMHNCWMRNVGGRLESRYRYSASLVYNTFPWIQPNEKQSKAIEEAAFAI LKARSNYPNESLAGLYDPKTMPSELLKAHQKLDKAVDSVYGFKGPNTEIARIAFLFETYQKMTSLLPPEK EIKKSKGKN Q47112.2 Colicin-E7 11 >gi|12644448|sp|Q47112.2|CEA7_ECOLX RecName: Full = Colicin-E7 (CEA7_ECOLX) MSGGDGRGHNSGAHNTGGNINGGPTGLGGRGGASDGSGWSSENNPWGGGSGSGVHWGGGSGHGNGGGNSN SGGGSNSSVAAPMAFGFPALAAPGAGTLGISVSGEALSAAIADIFAALKGPFKFSAWGIALYGILPSEIA KDDPNMMSKIVTSLPAETVTNVQVSTLPLDQATVSVTKRVTDVVKDTRQHIAVVAGVPMSVPVVNAKPTR TPGVFHASFPGVPSLTVSTVKGLPVSTTLPRGITEDKGRTAVPAGFTFGGGSHEAVIRFPKESGQKPVYV SVTDVLTPAQVKQRQDEEKRLQQEWNDAHPVEVAERNYEQARAELNQANKDVARNQERQAKAVQVYNSRK SELDAANKTLADAKAEIKQFERFAREPMAAGHRMWQMAGLKAQRAQTDVNNKKAAFDAAAKEKSDADVAL SSALERRKQKENKEKDAKAKLDKESKRNKPGKATGKGKPVNNKWLNNAGKDLGSPVPDRIANKLRDKEFK SFDDFRKKFWEEVSKDPELSKQFSRNNNDRMKVGKAPKTRTQDVSGKRTSFELHHEKPISQNGGVYDMDN ISVVTPKRHIDIHRGK CAA38134.1 EndA 12 >gi|47374|emb|CAA38134.1| EndA [Streptococcus pneumoniae] MNKKTROTLIGLLVLLLLSTGSYYIKQMPSAPNSPKTNLSQKKQASEAPSQALAESVLTDAVKSQIKGSL EWNGSGAFIVNGNKTNLDAKVSSKPYADNKTKTVGKETVPTVANALLSKATRQYKNRKETGNGSTSWTPP GWHQVKNLKGSYTHAVDRGHLLGYALIGGLDGFDASTSNPKNIAVQTAWANQAQAEYSTGQNYYESKVRK ALDQNKRVRYRVTLYYASNEDLVPSASQIEAKSSDGELEFNVLVPNVQKGLQLDYRTGEVTVTQ P25736.1 Endo I 13 >gi|119325|sp|P25736.1|END1_ECOLI RecName: Full = Endonuclease-1; (END1_ECOLI) AltName: Full = Endonuclease I; Short = Endo I; Flags: Precursor MYRYLSIAAVVLSAAFSGPALAEGINSFSQAKAAAVKVHADAPGTFYCGCKINWQGKKGVVDLQSCGYQV RKNENRASRVEWEHVVPAWQFGHQRQCWQDGGRKNCAKDPVYRKMESDMHNLQPSVGEVNGDRGNFMYSQ WNGGEGQYGQCAMKVDFKEKAAEPPARARGAIARTYFYMRDQYNLTLSRQQTQLFNAWNKMYPVTDWECE RDERIAKVQGNHNPYVQRACQARKS Q14249.4 Human Endo G 14 >gi|317373579|sp|Q14249.4|NUCG_HUMAN RecName: Full = Endonuclease G, (NUCG_HUMAN) mitochondrial; Short = Endo G; Flags: Precursor MRALRAGLTLASGAGLGAVVEGWRARREDARAAPGLLGRLPVLPVAAAAELPPVPGGPRGPGELAKYGLP GLAQLKSRESYVLCYDPRTRGALWVVEQLRPERLRGDGDRRECDFREDDSVHAYHRATNADYRGSGFDRG HLAAAANHRWSQKAMDDTFYLSNVAPQVPHLNQNAWNNLEKYSRSLTRSYQNVYVCTGPLFLPRTEADGK SYVKYQVIGKNHVAVPTHFFKVLILEAAGGQIELRTYVMPNAPVDEAIPLERFLVPIESIERASGLLFVP NILARAGSLKAITAGSK P38447.1 Bovine Endo G 15 >gi|585596|sp|P38447.1|NUCG_BOVIN RecName: Full = Endonuclease G, (NUCG_BOVIN) mitochondrial; Short = Endo G; Flags: Precursor MQLLRAGLTLALGAGLGAAAESWWRQRADARATPGLLSRLPVLPVAAAAGLPAVPGAPAGGGPGELAKYG LPGVAQLKSRASYVLCYDPRTRGALWVVEQLRPEGLRGDGNRSSCDFHEDDSVHAYHRATNADYRGSGFD RGHLAAAANHRWSQKAMDDTFYLSNVAPQVPHLNQNAWNNLEKYSRSLTRTYQNVYVCTGPLFLPRTEAD GKSYVKYQVIGKNHVAVPTHFFKVLILEAAGGQIELRSYVMPNAPVDEAIPLEHFLVPIESIERASGLLF VPNILARAGSLKAITAGSK AAW33811.1 R.HinP1I 16 >gi|57116674|gb|AAW33811.1| R.HinP1I restriction endonuclease [Haemophilus influenzae] MNLVELGSKTAKDGFKNEKDIADRFENWKENSEAQDWLVTMGHNLDEIKSVKAVVLSGYKSDINVQVLVF YKDALDIHNIQVKLVSNKRGFNQIDKHWLAHYQEMWKFDDNLLRILRHFTGELPPYHSNTKDKARMFMTE FSQEEQNIVLNWLEKNRVLVLTDILRGRGDFAAEWVLVAQKVSNNARWILRNINEVLQHYGSGDISLSPR GSINFGRVTIQRKGGDNGRETANMLQFKIDPTELFDI AAO93095.1 I-BasI 17 >gi|29838473|gb|AAO93095.1| I-BasI [Bacillus phage Bastille] MFQEEWKDVTGFEDYYEVSNKGRVASKRTGVIMAQYKINSGYLCIKFTVNKKRTSHLVHRLVAREFCEGY SPELDVNHKDTDRMNNNYDNLEWLTRADNLKDVRERGKLNTHTAREALAKVSKKAVDVYTKDGSEYIATY PSATEAAEALGVQGAKISTVCHGKRQHTGGYHFKFNSSVDPNRSVSKK AAK09365.1 I-BmoI 18 >gi|12958590|gb|AAK09365.1|AF321518_2 intron encoded I-BmoI [Bacillus mojavensis] MKSGVYKITNKNTGKFYIGSSEDCESRLKVHFRNLKNNRHINRYLNNSFNKHGEQVFIGEVIHILPIEEA IAKEQWYIDNFYEEMYNISKSAYHGGDLTSYHPDKRNIILKRADSLKKVYLKMTSEEKAKRWQCVQGENN PMFGRKHTETTKLKISNHNKLYYSTHKNPFKGKKHSEESKTKLSEYASQRVGEKNPFYGKTHSDEFKTYM SKKFKGRKPKNSRPVIIDGTEYESATEASRQLNVVPATILHRIKSKNEKYSGYFYK P34081.1 I-HmuI 19 >gi|465641|sp|P34081.1|HMUI_BPSP1 RecName: Full = DNA endonuclease I- HmuI; AltName: Full = HNH homing endonuclease I-HmuI MEWKDIKGYEGHYQVSNTGEVYSIKSGKTLKHQIPKDGYHRIGLFKGGKGKTFQVHRLVAIHFCEGYEEG LVVDHKDGNKDNNLSTNLRWVTQKINVENQMSRGTLNVSKAQQIAKIKNQKPIIVISPDGIEKEYPSTKC ACEELGLTRGKVTDVLKGHRIHHKGYTFRYKLNG P13299.2 I-TevI 20 >gi|6094464|sp|P13299.2|TEV1_BPT4 RecName: Full = Intron-associated endonuclease 1; AltName: Full = I-TevI; AltName: Full = IRF protein MKSGIYQIKNTLNNKVYVGSAKDFEKRWKRHFKDLEKGCHSSIKLQRSFNKHGNVFECSILEEIPYEKDL IIERENFWIKELNSKINGYNIADATFGDTCSTHPLKEEIIKKRSETVKAKMLKLGPDGRKALYSKPGSKN GRWNPETHKFCKCGVRIQTSAYTCSKCRNRSGENNSFFNHKESDITKSKISEKMKGKKPSNIKKISCDGV IFDCAADAARHFKISSGLVTYRVKSDKWNWFYINA P07072.2 I-TevII 21 >gi|20141823|sp|P07072.2|TEV2_BPT4 RecName: Full = Intron-associated endonuclease 2; AltName: Full = I-TevII MKWKLRKSLKIANSVAFTYMVRFPDKSFYIGFKKFKTIYGKDTNWKEYNSSSKLVKEKLKDYKAKWIILQ VFDSYESALKHEEMLIRKYFNNEFILNKSIGGYKFNKYPDSEEHKQKLSNAHKGKILSLKHKDKIREKLI EHYKNNSRSEAHVKNNIGSRTAKKTVSIALKSGNKFRSFKSAAKFLKCSEEQVSNHPNVIDIKITIHPVP EYVKINDNIYKSFVDAAKDLKLHPSRIKDLCLDDNYPNYIVSYKRVEK Q38419.1 I-TevIII 22 >gi|11387192|sp|Q38419.1|TEV3_BPR03 RecName: Full = Intron-associated endonuclease 3; AltName: Full = I-TevIII MNYRKIWIDANGPIPKDSDGRTDEIHHKDGNRENNDLDNLMCLSIQEHYDIHLAQKDYQACHAIKLRMKY SPEEISELASKAAKSREIQIFNIPEVRAKNIASIKSKIENGTFHLLDGEIQRKSNLNRVALGIHNFQQAE HIAKVKERNIAAIKEGTHVFCGGKMQSETQSKRVNDGSHHFLSEDHKKRTSAKTLEMVKNGTHPAQKEIT CDFCGHIGKGPGFYLKHNDRCKLNPNRIQLNCPYCDKKDLSPSTYKRWHGDNCKARFND AAM00817.1 I-TwoI 23 >gi|19881200|gb|AAM00817.1|AF485080_2 HNH endonuclease I-TwoI [Staphylococcus phage Twort] MEELWKEIPGFNSYMISNKGQVYSRKANKILALRTDKNGYKRISIFNNEGKRILLGVHKLVLLGFKGINT EKPIPHHKNNIKDDNRLENLEWVTVSENTKHAYDIGALKSPRRVTCTLYYKGEPLSCYDSLFDLAKALKV SRSVIESPRNGLVLSTFEVKREPTIQGLPLNKEIFEHSLIKGLGNPPLKVYNEDETYYFLTLMDISKYFN ESYSKVQRGYYKGKWKSYIIEHIDFYEYYKQTH P11405.1 R.MspI 24 >gi|135239|sp|P11405.1|T2M1_MORSP RecName: Full = Type-2 restriction enzyme MspI; Short = R.MspI; FatName: Full = Endonuclease MspI; AltName: Full = Type II restriction enzyme MspI MRTELLSKLYDDFGIDQLPHTQHGVTSDRLGKLYEKYILDIFKDIESLKKYNTNAFPQEKDISSKLLKAL NLDLDNIIDVSSSDTDLGRTIAGGSPKTDATIRFTFHNQSSRLVPLNIKHSSKKKVSIAEYDVETICTGV GISDGELKELIRKHQNDQSAKLFTPVQKQRLTELLEPYRERFIRWCVTLRAEKSEGNILHPDLLIRFQVI DREYVDVTIKNIDDYVSDRIAEGSKARKPGFGTGLNWTYASGSKAKKMQFKG R.MvaI R.MvaI 25 >gi|119392963|gb|AAM03024.2|AF472612_1 R.MvaI [Kocuria varians] MSEYLNLLKEAIQNVVDGGWHETKRKGNTGIGKTFEDLLEKEEDNLDAPDFHDIEIKTHETAAKSLLTLF TKSPTNPRGANTMLRNRYGKKDEYGNNILHQTVSGNRKTNSNSYNYDFKIDIDWESQVVRLEVFDKQDIM IDNSVYWSFDSLQNQLDKKLKYIAVISAESKIENEKKYYKYNSANLFTDLTVQSLCRGIENGDIKVDIRI GAYHSGKKKGKTHDHGTAFRINMEKLLEYGEVKVIV CAA45962.1 NucA 26 gi|39041|emb|CAA45962.1| NucA [Nostoc sp. PCC 7120] MGICGKLGVAALVALIVGCSPVQSQVPPLTELSPSISVELLLGNPSGATPTKLTPDNYLMVXNQYALSYN NSKGTANWVAWQLNSSWLGNAERQDNFRPDKTLPAGWVRVTPSMYSGSGYDRGHIAPSADRTKTTEDNAA TFLMTNMMPQTPDNNRNTWGNLEDYCRELVSQGKELYIVAGPNGSLGKPLKGKVTVPKSTWKIVVVLDSP GSGLEGITANTRVIAVNIPNDPELNNDWRAYKVSVDELESLTGYDFLSNVSPNIQTSIESKVDN P37994.2 NucM 27 gi|313104150|sp|P37994.2|NUCM_DICD3 RecName: Full Nuclease nucM; Flags: Precursor MLRNLVIFAVLGAGLTTLAAAGQDINNFTQAKAAAAKIHQDAPGTFYCGCKINWQGKKGTPDLASCGYQV RKDANRASRIEWEHVVPAWQFGHQRQCWQDGGRKNCTKDDVYRQIETDLHNLQPAIGEVNGDRGNFMYSQ WNGGERQYGQCEMKIDFKSQLAEPPERARGAIARTYFYMRDRYNLNLSRQQTQLFDAWNKQYPATTWECT REKRIAAVQGNHNPYVQQACQP AAF19759.1 Vvn 28 >gi|6635279|gb|AAF19759.1|AF063303_1 nuclease precursor Vvn [Vibrio vulnificus] MKRLFIFIASFTAFAIQAAPPSSFSAAKQQAVKIYQDHPISFYCGCDIEWQGKKGIPNLETCGYQVRKQQ TRASRIEWEHVVPAWQFGHHRQCWQKGGRKNCSKNDQQFRLMEADLHNLTPAIGEVNGDRSNFNFSQWNG VDGVSYGRCEMQVNFKQRKVMPQTELRGSIARTYLYMSQEYGFQLSKQQQQLMQAWNKSYPVDEWECTRD DRIAKIQGNHNPFVQQSCQTQ AAF19759.1 Vvn_CLS 29 >Vvn_CLS (variant of AAF19759.1) (reference) MASGAPPSSFSAAKQQAVKIYQDHPISFYCGCDIEWQGKKGIPNLETCGYQVRKQQTRASRIEWEHVVPA WQFGHHRQCWQKGGRKNCSKNDQQFRLMEADLHNLTPAIGEVNGDRSNFNFSQWNGVDGVSYGRCEMQVN FKQRKVMPPDRARGSIARTYLYMSQEYGFQLSKQQQQLMQAWNKSYPVDEWECTRDDRIAKIQGNHNPFV QQSCQTQGSSAD P00644.1 Staphylococcal 30 >gi|128852|sp|P00644.1|NUC_STAAU RecName: Full = Thermonuclease; nuclease Short = TNase; AltName: Full = Micrococcal nuclease; AltName: (NUC_STAAU) Full = Staphylococcal nuclease; Contains: RecName: Full = Nuclease B; Contains: RecName: Full = Nuclease A; Flags: Precursor MLVMTEYLLSAGICMAIVSILLIGMAISNVSKGQYAKREFFFATSCLVLTLVVVSSLSSSANASQTDNGV NRSGSEDPTVYSATSTKKLHKEPATLIKAIDGDTVKLMYKGQPMTFRLLLVDTPETKHPKKGVEKYGPEA SAFTKKMVENAKKIEVEFDKGQRTDKYGRGLAYIYADGKMVNEALVRQGLAKVAYVYKPNNTHEQHLRKS EAQAKKEKLNIWSEDNADSGQ P43270.1 Staphylococcal 31 >gi|1171859|sp|P43270.1|NUC_STAHY RecName: Full = Thermonuclease; nuclease Short = TNase; AltName: Full = Micrococcal nuclease; AltName: (NUC_STAHY) Full = Staphylococcal nuclease; Flags: Precursor MKKITTGLIIVVAAIIVLSIQFMTESGPFKSAGLSNANEQTYKVIRVIDGDTIIVDKDGKQQNLRMIGVD TPETVKPNTPVQPYGREASDETKRHLTNQKVALEYDKQEKDRYGRTLAYVWLGKEMENEKLAKEGLARAK FYRPNYKYQERIEQAQKQAQKLKKNIWSN P29769.1 Micrococcal 32 >gi|266681|sp|P29769.1|NUC_SHIFL RecName: Full = Micrococcal nuclease; nuclease Flags: Precursor (NUC_SHIFL) MKSALAALRAVAAAVVLIVSVPAWADFRGEVVRILDGDTIDVLVNRQTIRVRLADIDAPESGQAFGSRAR QRLADLTFRQEVQVTEKEVDRYGRTLGVVYAPLQYPGGQTQLTNINAIMVQEGMAWAYRYYGKPTDAQMY EYEKEARRQRLGLWSDPNAQEPWKWRRASKNATN P94492.1 Endonuclease 33 gi|81345826|sp||YNCB_BACSU RecName: Full = Endonuclease yncB; Flags: yncB Precursor MKKILISMIAIVLSITLAACGSNHAAKNHSDSNGTEQVSQDTHSNEYNQTEQKAGTPHSKNQKKLVNVTL DRAIDGDTIKVIYNGKKDTVRYLLVDTPETKKPNSCVQPYGEDASKRNKELVNSGKLQLEFDKGDRRDKY GALLAYVYVDGKSVQETLLKEGLARVAYVYEPNTKYIDQFRLDEQEAKSDKLSIWSKSGYVTNRGFNGCV K P00641.1 Endodeoxy- 34 >gi|119370|sp|P00641.1|ENRN_BPT7 RecName: Full = Endodeoxyribonuclease ribonu- 1; AltName: Full = Endodeoxyribonuclease I; Short = Endonuclease clease I MAGYGAKGIRKVGAFRSGLEDKVSKQLESKGIKFEYEEWKVPYVIPASNHTYTPDFLLPNGIFVETKGLW (ENRN_BPT7) ESDDRKKHLLIREQHPELDIRIVFSSSRTKLYKGSPTSYGEFCEKHGIKFADKLIPAEWIKEPKKEVPFD RLKRKGGKK Q53H47.1 Metnase 35 >gi|74740552|sp|Q53H47.1|SETMR_HUMAN RecName: Full = Histone-lysine N- methyltransferase SETMAR; AltName: Full = SET domain and mariner transposase fusion gene-containing protein; Short = HsMar1; Short = Metnase; Includes: RecName: Full = Histone-lysine N-methyl- transferase; Includes: RecName: Full = Mariner transposase Hsmar1 MAEFKEKPEAPTEQLDVACGQENLPVGAWPPGAAPAPFQYTPDHVVGPGADIDPTQITFPGCICVKTPCL PGTCSCLRHGENYDDNSCLRDIGSGGKYAEPVFECNVLCRCSDHCRNAVVQKGLQFHFQVFKTHKKGWGL RTLEFIPKGRFVCEYAGEVLGFSEVQRRIHLQTKSDSNYIIAIREHVYNGQVMETFVDPTYIGNIGRFLN HSCEPNLLMIPVRIDSMVPKLALFAAKDIVPEEELSYDYSGRYLNLTVSEDKERLDHGKLRKPCYCGAKS CTAFLPFDSSLYCPVEKSNISCGNEKEPSMCGSAPSVFPSCKRLTLETMKMMLDKKQIRAIFLFEFKMGR KAAETTRNINNAFGPGTANERTVQWWFKKFCKGDESLEDEERSGRPSEVDNDQLRAIIEADPLTTTREVA EELNVNHSTVVRHLKQIGKVKKLDKWVPHELTENQKNRRFEVSSSLILRNHNEPFLDRIVTCDEKWILYD NRRRSAQWLDQEEAPKHFPKPILHPKKVMVTIWWSAAGLIHYSFLNPGETITSEKYAQEIDEMNQKLQRL QLALVNRKGPILLHDNARPHVAQPTLQKLNELGYEVLPHPPYSPDLLPTNYHVFKHLNNFLQGKRFHNQQ DAENAFQEFVESQSTDFYATGINQLISRWQKCVDCNGSYFD ABD15132.1 Nb.BsrDI 36 >gi|86757493|gb|ABD15132.1| Nb.BSrDI [Geobacillus stearothermophilus] MTEYDLHLYADSFHEGHWCCENLAKIAQSDGGKHQIDYLQGFIPRHSLIFSDLIINITVFGSYKSWKHLP KQIKDLLFWGKPDFIAYDPKNDKILFAVEETGAVPTGNQALQRCERIYGSARKQIPFWYLLSEFGQHKDG GTRRDSIWPTIMGLKLTQLVKTPSIILHYSDINNPEDYNSGNGLKFLFKSLLQIIINYCTLKNPLKGMLE LLSIQYENMLEFIKSQWKEQIDFLPGEEILNTKTKELARMYASLAIGQTVKIPEELFNWPRTDKVNFKSP QGLIKYDELCYQLEKAVGSKKAYCLSNNAGAKPQKLESLKEWINSQKKLFDKAPKLTPPAEFNMKLDAFP VTSNNNYYVTTSKNILYLFDYWKDLRIAIETAFPRLKGKLPTDIDEKPALIYICNSVKPGRLFGDPFTGQ LSAFSTIFGKKNIDMPRIVVAYYPHQIYSQALPKNNKSNKGITLKKELTDFLIFHGGVVVKLNEGKAY ABD15133.1 BsrDI A 37 gi|86757494|gb|ABD15133.1| BsrDI A [Geobacillus stearothermophilus] MTDYRYSFELSEEIARWAFEIKTKNTDWFVAFSNPTAGPWKRVMAIDKASNREGEVHRFGREDERPDIIL VNDNISLILILEAKEKLNQLISKSQVDKSVDVFLTLSSILKEKSDNNYWGDRTKYINVLGILWGSEQETS QKDIDNAFRVYRDSLVKNLKEINPTPTNICTDILVGVESIKNKKEEISIKIHVSNIYAEIYPKFTGKHLL EKLAVLN ABN42182.1 Nt.BspD6I 38 gi|125396996|gb|ABN42182.1| heterodimeric restriction endonuclease (R.BspD6I R.BspD6I large subunit [Bacillus sp. D6] large MAKKVNWYVSCSPRSPEKIQPELKVLANFEGSYWKGVKGYKAQEAFAKELAALPQFLGTTYKKEAAFSTR subunit) DRVAPMKTYGFVFVDEEGYLRITEAGKMLANNRRPKDVFLKQLVKWQYPSFQHKGKEYPEEEWSINPLVF VLSLLKKVGGLSKLDIAMFCLTATNNNQVDEIAEEIMQFRNEREKIKGQNKKLEFTENYFFKRFEKIYGN VGKIREGKSDSSHKSKIETKMANARDVADATTRYFRYTGLEVARGNQLVLNPEKSDLIDEIISSSKVVKN YTRVEEFHEYYGNPSLPQFSFETKEQLLDLAHRIRDENTRLAEQLVEHFPNVRVEIQVLEDIYNSLNKKV DVETLKDVIYHAKELQLELKKKKLQADFNDPRQLEEVIDLLEVYHEKKNVIEEKIKARFIANKNTVFEWL TWNGFIILGNALEYKNNFVIDEELQPVTHAAGNQPDMEIIYEDFIVLGEVTTSKGATQFKMESEPVTRHY LNKKKELEKQGVEKELYCLFIAPEINKNTFEEFMKYNIVQNTRIIPLSLKQFNMLLMVQKKLIEKGRRLS SYDIKNLMVSLYRTTIECERKYTQIKAGLEETLNNWVVDKEVRF ABN42183.1 ss.BspD6I 39 >gi|125396997|gbABN42183.1| heterodimeric restriction endonuclease (R.BspD6I R.BspD6I small subunit [Bacillus sp. D6] small MQDILDFYEEVEKTINPPNYFEWNTYRVFKKLGSYKNLVPNFKLDDSGHPIGNAIPGVEDILVEYEHFSI subunit) LIECSLTIGEKQLDYEGDSVVRHLQEYKKKGIEAYTLFLGKSIDLSFARHIGFNKESEPVIPLTVDQFKK LVTQLKGDGEHFNPNKLKEILIKLLRSDLGYDQAEEWLTFIEYNLK AAK27215.1 R.PleI 40 >gi|13448813|gb|AAK27215.1|AF355461_2 restriction endonuclease R.PleI [Paucimonas lemoignei] MAKPIDSKVLFITTSPRTPEKMVPEIELLDKNFNGDVWNKDTQTAFMKILKEESFFDGEGKNDPAFSARD RINRAPKSLGFVILTPKLSLTDAGVELIKAKRKDDIFLRQMLKFQLPSPYHKLSDKAALFYVKPYLEIFR LVRHFGSLTFDELMIFGLQIIDFRIFNQIVDKIEDFRVGKIENKGRYKTYKKERFEEELGKIYKDELFGL TEASAKTLITKKGNNMRDYADACVRYLRATGMVNVSYQGKSLSIVQEKKEEVDFFLKNTEREPCFINDEA SYVSYLGNPNYPKLFVDDVDRIKKKLRFDFKKTNKVNALTLPELKEELENEILSRKENILKSQISDIKNF KLYEDIQEVFEKIENDRTLSDAPLMLEWNTWRAMTMLDGGEIKANLKFDDFGSPMSTAIGNMPDIVCEYD DEQLSVEVTMASGQKQYEMEGEPVSRHLGKLKKSSEKPVYCLFIAPKINPSSVANFFMSHKVDIEYYGGK SLIIPLELSVFRKMIEDTFKASYIPKSDNVHKLFKNFASIADEAGNEKVWYEGVKRTAMNWLSLS AAK39546.1 MlyI 41 >gi|13786046|gb|AAK39546.1|AF355462_2 MlyIR [Micrococcus lylae] MASLSKTKHLFGFTSPRTIEKIIPELDILSQQFSGKVWGENQINFFDAIFNSDFYEGTTYPQDPALAARD RITRAPKALGFIQLKPVIQLTKAGNQLVNQKRLPELFTKQLLKFQLPSPYHTQSPTVNFNVRPYLELLRL INELGSISKTEIALFFLQLVNYNKFDEIKNKILKFRETRKNNRSVSWKTYVSQEFEKQISIIFADEVTAK NFRTRESSDESFKKFVKTKEGNMKDYADAFFRYIRGTQLVTIDKNLHLKISSLKQDSVDFLLKNTDRNAL NLSLMEYENYLFDPDQLIVLEDNSGLINSKIKQLDDSINVESLKIDDAKDLLNDLEIQRKAKTIEDTVNH LKLRSDIEDILDVFAKIKKADVPDVPLFLEWNIWRAFAALNHTQAIEGNFIVDLDGMPLNTAPGKKPDIE INYGSFSCIVEVPMSSGETQFNMEGSSVPRHYGDLVRKVDHDAYCIFIAPKVAPGTKAHFFNLNRLSTKH YGGKTKIIPMSLDDFICFLQVGITHNFQDINKLKNWLDNLINFNLESEDEEIWFEEIISKISTWAI YP_ AlwI 42 >gi|319768594|ref|YP_004134094.1| restriction endonuclease, type II, 004134094.1 AlwI [Geobacillus sp. Y412MC52] MNKKNTRKVWFITRPERDPRFHQEALLALQKATDDFRLKWAGNREVEKRYEEELANMGIKRNNVSHDGSG GRTWMAMLKTFSYCYVDDDGYIRLTKVGEKLIQGEKVYENTRKQVLTLQYPNAYFLEPGFRPKFDEGFRI RPVLFLIKLANDERLDFYVTKEEITYFAMTAQKDSQLDEIVHKILAFRKAGPREREEMKQDIAAKFDHRE RSDKGARDFYEAHSDVAHTFMLISDYTGLVEYIRGKALKGDSSKINEIKQEIAEIEKRYPFNTRYMISLE RMAENSGLDVDSYKASRYGNIKPAANSSKLRAKAERILAQFPSIESMSKEEIAGALQKYLSPRDIEKVIH EIVENKDDFEGINSDFVETYLNEKDNLAFEDKTGQIFSALGFDVAMRPKAKNGERTEIEIIARYGGSKFG IIDAKNYAGKFPLSSSLVSHMASEYIPNYTGYEGKELTFFGYVTANDFSGERNLEKISDKAKRITGNPIS GFLVTARTLLGFLDYCIENDVPLEDRAELFVKAVKNKGYKSLEALLRELKETI AAY97906.1 Mva1269I 43 >gi|68480350|gb|AAY97906.1| Mva1269I restriction endonuclease [Kocuria varians] MYLNTAVFNIYGDNIVECSRAFHYILEGFKLANISITQEYDLQNITTPKFCIYTDKFRYIFIFIPGTSAS RWNKDIYKELVLNNGGPLKEGADAIITRIFSEDSELVLASMEFSAALPAGNNTWQRSGRAYSLTAANIPY FYIVQLGGKEIKKGKDGKSDKFATRLPNPALSLSFTLNTIKKPAPSLIVYDQAPEADSAISDLYSNCYGI DDFSLYLFKLITEENNLHELKNIYNKNVEFLQLRSVDEKGKNFSGKDYKYIFEHKDPYKGLTEVVKERKI PWKKKTATKTFENFPLRNQAPIFRLIDFLSTKSYGIVSKDSLPLTFIPSEHRVEVANYICNQLYIDKVSD EFVKWIYKKEDLAICIINGFKPGGDDSRPDRGLPPFTKMLTNLDILTLMFGPAPPTQWDYLDSDPEKLNK TNGLWQSIFAFSDAILVDSSTRDNNKFVYNAYLKEHWVVQREKKESNTPISYFPKSVGEHDVDTSLHILF TYIGKHFESACNPPGGDWSGVSLLKNNIEYRWTSMYRVSQDGTKRPDHIYQLVYNSTDTLLLIESKGIKN DLLKSKEANVGIGMINYLKNLMARDYTAVKKDGEWKNIHGQMTLDKFLTFSAVAYLFTTDFDNEYTSAAE LLVHSNTQLAFALEIKEKNSVMHIFTANTVAYNFAEYLLETMRNSHLPLKIYKPI ADR72996.1 BsrI 44 >gi|313667100|gb|ADR72996.1| BsrI [Geobacillus stearothermophilus] MRNIRIYSEVKEQGIFFKEVIQSVLEKANVEVVLVNSAMLDYSDVSVISLIRNQKKFDLLVSEVRDKREI PIVMVEFSTAVTTDDHELQRADAMFWAYKYKIPYLKISPMEKKSQTADDKFGGGRLLSVNDQIIHMYRTD GVMYHIEWESMDNSAYVKNAELYPSCPDCAPELASLFRCLLETIEKCENIEDYYRILLDKLGKQKVAVKW GNFREEKTLEQWKHEKFDLLERFSKSSSRMEYDKDKKELKIKVNRYGHAMDPERGILAFWKLVLGDEWKI VAEFQLQRKTLKGRQSYQSLFDEVSQEEKLMNIASEIIKNGNVISPDKAIEIHKLATSSTMISTIDLGTP ERKYITDDSLKGYLQHGLITNIYKNLLYYVDEIRFTDLQRKTIASLTWNKEIVNDYYKSLMDQLLDKNLR VLPLTSIKNISEDLITWSSKEILINLGYKILAASYPEAQGDRCILVGPTGKKTERKFIDLIAISPKSKGV ILLECKDKLSKSKDDCEKMNDLLNHNYDKVTKLINVLNINNYNYNNIIYTGVAGLIGRKNVDNLPVDFVI KFKYDAKNLKLNWEINSDILGKHSGSFSMEDVAVVRKRS AAL86024.1 BsmI 45 >gi|19347662|gb|AAL86024.1| BsmI [Geobacillus stearothermophilus] MNVFRINGDNIIECERVIDLILSKINPQKVKRGFISLSCPFIEIIFKEGHDYFHWRFDMFPGFNKNTNDR WNSNILDLLSQKGSFLYETPDVIITSLNNGKEEILMAIEFCSALQAGNQAWQRSGRAYSVGRTGYPYIYI VDFVKYELNNSDRSRKNLRFPNPAIPYSYISHSKNTGNFIVQAYFRGEEYQPKYDKKLKFFDETIFAEDD IADYIIAKLQHRDTSNIEQLLINKNLKMVEFLSKNTKNDNNFTYSEWESIYNGTYRITNLPSLGRFKFRK KIAEKSLSGKVKEENNIVQRYSVGLASSDLPFGVIRKESANDFINDVCKLYNINDMKIIKELKEDADLIV CMLKGFKPRGDDNRPDRGALPLVAMLAGENAQIFTFIYGPLIKGAINLIDQDINKLAKRNGLWKSFVSLS DFIVLDCPIIGESYNEFRLIINKNNKESILRKTSKQQNILVDPTPNHYQENDVDTVIYSIFKYIVPNCFS GMCNPPGGDWSGLSIIRNGHEFRWLSLPRVSENGKRPDHVIQILDLFEKPLLLSIESKEKPNDLEPKIGV QLIKYIEYLFDFTPSVQRKIAGGNWEFGNKSLVPNDFILLSAGAFIDYDNLTENDYEKIFEVTGCDLLIA IKNQNNPQKWVIKFKPKNTIAEKLVNYIKLNFKSNIFDTGFFHIEG ADI24225.1 Nb.BtsCI 46 >gi|297185870|gb|AD124225.1| BtsCI bottom-strand nicking enzyme variant [synthetic construct] MKRILYLLTEERPKINIIHQIINLEYKATLHFGAKIVPVMNEENKFTFIYHVKGIEVEGFDAVLIKIVSG HSSFVDYLVFDSNDLKPEKNTITLFDLDQYELDLSYYFGKGWIVRIPSPSDLPKYVVEETKTDDHESRNT NAYQRSSKFVFCELYYGKEVKKYMLYDISDGRTLSGTDTHNFGMRMLVTNNVNLVGVPNMYLPFTDIKEF INEKNRIADNGPSHNVPIRLKLDKEKNVIYISAKLDKGNGKNKNKISNDPNIGAVAIISATLANLNWKGD IEIINHNLLPSSISSRSNGNKLLYIMKKLGVRFNNINVNWNNIKNNINYFFYNITSEKIVSIYYHLYVED KLSNARVIFDNHAGCGKSYFRTLNNKIIPVGKEIPLPALVIFDSDQNIVKVIAAAKAENVYNGVEQLSTF DKFIESYINKYYPGAAVECSVITWGKSSNPYVSFYLDKDGSAVFL ADI242241 Nt.BtsCI 47 >gi|297185868|gb|ADI24224.1| BtsCI top-strand nicking enzyme variant [synthetic construct] MKRILYLLTEERPKINIIHQIINLEYKATLHFGAKIVPVMNEENKFTFIYHVKGIEVEGFDAVLIKIVSG HSSFVDYLVFDSNDLKPEKNTITLFDLDQYELDLSYYFGKGWIVRIPSPSDLPKYVVFETKTDDHESRNT NAYQRSSKFVFCELYYGKEVKKYMLYDISDGRTLSGTDTHNFGMRMLVTNNVNLVGVPNMYLPFTDIKEF INEKNRIADNGPSHNVPIRLKLDKEKNVIYISAKLDKGNGKNKNKISNDPNIGAVAIISATLRNLNWKGD IEIINENLLPSSISSRSNGNKLLYIMKKLGVRFNNINVNWNNIKNNINYFFYNITSEKIVSIYYHLYVED KLSNARVIFDNHAGCGKSYFRTLNNKIIPVGKEIPLPDLVIFDSDQNIVKVIEAEKAENVYNGVEQLSTF DKFIESYINKYYPGAAVECSVITWGKSSNPYVSFYLDKDGSAVFL >gi|85720924|gb|ABC75874.1| R1.BtsI [Geobacillus thermoglucosidasius] MKITEGIVHVAMRHFLKSNGWKLIAGQYPGGSDDELTALNIVDPVVARDNSPDPRRHSLGKIVPDLIAYK NDDLLVIEAKPKYSQDDRDKLLYLLSERKHDFYAALEKFATERNHPELLPVSKLNIIPGLAFSASENKFK KDPGFVYIRVSGIFEAFMEGYDWG ABC758741 R1.BtsI 48 >gi|85720924|gb|ABC75874.1| R1.BtsI [Geobacillus thermoglucosidasius] MKITEGIVHVAMRHFLKSNGWKLIAGQYPGGSDDELTALNIVDPVVARDNSPDPRRHSLGKIVPDLIAYK NDDLLVIEAKPKYSQDDRDKLLYLLSERKHDFYAALEKFATERNHPELLPVSKLNIIPGLAFSASENKFK KDPGFVYIRVSGIFEAFMEGYDWG ABC75876.1 R2.BtsI 49 >gi|85720926|gb|ABC75876.1| R2.BtsI [Geobacillus thermoglucosidasius] MQIEQLMKSLTIYFDDIQEGLWFKNLHPLLESASLEAITGSLKRNPNLADVLKYDRPDIILTLNQTPILV IERTIEVPSGHNVGQRYGRLAAASEAGVPLVYFGPYAARKHGGATEGPRYMNLRLFYALDVMQKVNGSAI TTINWPVDQNFEILQDPSKDKRMKEYLEMFFDNLLKYGIAGINLAIRNSSFQAEQLAEREKFVETMITNP EQYDVPPDSVQILNAERFFNELGISENKRIICDEVVLYQVGMTYVRSDPYTGMALLYKYLYILGSERNRC LILKFPNITTDMWKKVAFGSRERKDVRIYRSVSDGILFADGYLSKEEL AAX146521 BbvCI 50 >gi|60202520|gb|AAX14652.1| BbvCI endonuclease subunit 1 subunit 1 [Brevibacillus brevis] MINEDFFIYEQLSHKKNLEQKGKNAFDEETEELVRQAKSGYHAFIEGINYDEVTKLDLNSSVAALEDYIS IAKEIEKKHKMFNWRSDYAGSIIPEFLYRIVHVATVKAGLKPIFSTRNTIIEISGAAHREGLQIRRKNED FALGFHEVDVKIASESHRVISLAVACEVKTNIDKNKLNGLDFSAERMKRTYPGSAYFLITETLDFSPDEN HSSGLIDEIYVLRKQVRTKNRVQKAPLCPSVFAELLEDILEISYRASNVKGHVYDRLEGGKLIRV AAX146531 BbvCI 51 >gi|60202521|gb|AAX14653.1| BbvCI endonuclease subunit 2 subunit 2 [Brevibacillus brevis] MFNQFNPLVYTHGGKLERKSKKDKTASKVFEEFGVMEAYNCWKEASLCIQQRDKDSVLKLVAALNTYKDA VEPIFDSRLNSAQEVLQPSILEEFFEYLFSRIDSIVGVNIPIRHPAKGYLSLSFNPHNIETLIQSPEYTV RAKDHDFIIGGSAKLTIQGHGGEGETTNIVVPAVAIECKRYLERNMLDECAGTAERLKRATPYCLYFVVA EYLKLDDGAPELTEIDEIYILRHQRNSERNKPGFKPNPIDGELIWDLYQEVMNHLGKIWWDPNSALQRGK VFNRP CAA74998.1 Bpu10I alpha 52 >gi|2894388|emb|CAA74998.1| Bpu10I restriction endonuclease alpha subunit subunit [Bacillus pumilus] MGVEQEWIKNITDMYQSPELIPSHASNLLHQLKREKRNEKLKKALEIITPNYISYISILLNNHNMTRKEI VILVDALNEYMNTLRHPSVKSVFSHQADFYSSVLPEFFNLLFRNLIKGLNEKIKVNSQKDIIIDCIFDPY NEGRVVFKKKRVDVAIILKNKFVFNNVEISDFAIPLVAIEIKTNLDKNMLSGIEQSVDSLKETFPLCLYY CITELADFAIEKQNYASTRIDEVFILRKQKRGPVARGTPLEVVHADLILEVVEQVGEHLSKFKDPIKTLK ARMTEGYLIKGKGK CAA74999.1 Bpu10I beta 53 >gi|2894389|emb|CAA74999.1| Bpu10I restriction endonuclease beta subunit subunit [Bacillus pumilus] MTQIDLSNTKHGSILFEKQKNVKEKYLQQAYKHYLYFRRSIDGLEITNDEAIFKLTQAANNYRDNVLYLF ESRPNSGQEAFRYTILEEFFYHLFKDLVKKKFNQEPSSIVMGKANSYVSLSFSPESFLGLYENPIPYIHT KDQDFVLGCAVDLKISPKNELNKENETEIVVPVIAIECKTYIERNMLDSCAATASRLKAAMPYCLYIVAS EYMKMDQAYPELTDIDEVFILCKASVGERTALKKKGLPPRKLDENLMVELFHMVERHLNRVWWSPNEALS RGRVIGRP ABM69266.1 BmrI 54 >gi|123187377|gb|ABM69266.1| BmrI [Bacillus megaterium] MNYFSLHPNVYATGRPKGLINMLESVWISNQKPGDGTMYLISGFANYNGGIRFYETFTEHINHGGKVIAI LGGSTSQRLSSKQVVAELVSRGVDVYIINRKRLLHAKLYGSSSNSGESLVVSSGNFTGPGMSQNVEASLL LDNNTTSSMGFSWNGMVNSMLDQKWQIHNLSNSNPTSPSWNLLYDERTTNLTLDDTQKVTLILTLGHADT ARIQAAPKSKAGEGSQYFWLSKDSYDFFPPLTIRNKRGTKATYSCLINMNYLDIKYIDSECRVTFEAENN FDFRLGTGKLRYTNVAASDDIAAITRVGDSDYELRIIKKGSSNYDALDSAAVNFIGNRGKRYGYIPNDEF GRIIGAKF CAC12783.1 BfiI 55 >gi|10798463|emb|CAC12783.1| restriction endonuclease BfiI [Bacillus firmus] MNFFSLHPNVYATGRPKGLIGMLENVWVSNHTPGEGTLYLISGFSNYNGGVRFYETFTEHINQGGRVIAI LGGSTSQRLSSRQVVEELLNRGVEVHIINRKRILHAKLYGTSNNLGESLVVSSGNFTGPGMSQNIEASLL LDNNTTQSMGFSWNDMISEMLNQNWHIHNMTNATDASPGWNLLYDERTTNLTLDETERVTLIVTLGHADT ARIQAAPGTTAGQGTQYFWLSKDSYDFFPPLTIRNRRGTKATYSSLINMNYIDINYTDTQCRVTFEAENN FDFRLGTGKLRYTGVAKSNDIAAITRVGDSDYELRIIKQGTPEHSQLDPYAVSFIGNRGKRFGYISNEEF GRIIGVTF P05725.1 1-CreI 1 >gi|140470|sp|P05725.1|DNE1_CHLRE RecName: Full = DNA endonuclease I- CreI; AltName: Full = 23S rRNA intron protein MNTKYNKEFLLYLAGFVDGDGSIIAQIKPNQSYKFKHQLSLAFQVTQKTQRRWFLDKLVDEIGVGYVRDR GSVSDYILSEIKPLHNFLTQLQPFLKLKQKQANLVLKIIWRLPSAKESPDKFLEVCTWVDQIAALNDSKT RKTTSETVRAVLDSLSEKKKSSP Q9UQ84.2 ExoI 56 >gi|85700954|sp|Q9UQ84.2|EXO1_HUMAN RecName: Full = Exonuclease 1; (EXO1_HUMAN) Short = hExo1; AltName: Full = Exonuclease I; Short = hExoI MGIQGLLQFIKEASEPIHVRKYKGQVVAVDTYCWLHKGAIACAEKLAKGEPTDRYVGFCMKFVNMLLSHG IKPILVFDGCTLPSKKEVERSRRERRQANLLKGKQLLREGKVSEARECFTRSINITHAMAHKVIKAARSQ GVDCLVAPYEADAQLAYLNKAGIVQAIITEDSDLLAFGCKKVILKMDQFGNGLEIDQARLGMCRQLGDVF TEEKFRYMCILSGCDYLSSLRGIGLAKACKVLRLANNPDIVKVIKKIGHYLKMNITVPEDYINGFIRANN TFLYQLVFDPIKRKLIPLNAYEDDVDPETLSYAGQYVDDSIALQIALGEKDINTFEQIDDYNPDTAMPAH SRSHSWDDKTCQKSANVSSIWHRNYSPRPESGTVSDAPQLKENPSTVGVERVISTKGLNLPRKSSIVKRP RSAELSEDDLLSQYSLSETKKTKKNSSEGNKSLSFSEVFVPDLVNGPTNKKSVSTPPRTRNKFATFLQRK NEESGAVVVPGTRSRFFCSSDSTDCVSNKVSIQPLDETAVTDKENNLHESEYGDQEGKRLVDTDVARNSS DDIPNNHIPGDHIPDKATVFTDEESYSFESSKFTRTISPPTLGTLRSCFSWSGGLGDFSRTPSPSPSTAL QQFRRKSDSPTSLPENNMSDVSQLKSEESSDDESHPLREEACSSQSQESGEFSLQSSNASKLSQCSSKDS DSEESDCNIKLLDSQSDQTSKLRLSHFSKKDTPLRNKVPGLYKSSSADSLSTTKIKPLGPARASGLSKKP ASIQKRKHHNAENKPGLQIKLNELWKNFGFKKDSEKLPPCKKPLSPVRDNIQLTPEAEEDIFNKPECGRV QRAIFQ P39875.2 Yeast ExoI 57 >gi|1706421|sp|P39875.2|EXO1_YEAST RecName: Full = Exodeoxyribo- (EXO1_YEAST) nuclease 1; AltName: Full = Exodeoxyribonuclease I; Short = EXO I; Short = Exonuclease I; AltName: Full = Protein DHS1 MGIQGLLPQLKPIQNPVSLRRYEGEVLAIDGYAWLHRAACSCAYELAMGKPTDKYLQFFIKRFSLLKTFK VEPYLVEDGDAIPVKKSTESKARDKRKENKAIAERLWACGEKKNAMDYFQKCVDITPEMAKCIICYCKLN GIRYIVAPFEADSQMVYLEQKNIVQGIISEDSDLLVFGCRRLITKLNDYGECLEICRDNFIKLPKKFPLG SLTNEEIITMVCLSGCDYTNGIPKVGLITAMKLVRRFNTIERIILSIQREGKLMIPDTYINEYEAAVLAF QFQRVFCPIRKKIVSLNEIPLYLKDTESKRKRLYACIGFVIHRETQKKQIVHFDDDIDHHLHLKIAQGDL NPYDFHQPLANREHKLQLASKSNIEFGKTNTTNSEAKVKPIESFFQKMTKLDHNPKVANNIHSLRQAEDK LTMAIKRRKLSNANVVQETLKDTRSKFFNKPSMTVVENFKEKGDSIQDFKEDTNSQSLEEPVSESQLSTQ IPSSFITTNLEDDDELSEEVSEVVSDIEEDRKNSEGKTIGNEIYNTDDDGDGDTSEDYSETAESRVPTSS TTSFPGSSQRSISGCTKVLQKFRYSSSFSGVNANRQPLFPRHVNQKSRGMVYVNQNRDDDCDDNDGKNQI TQRPSLRKSLIGARSQRIVIDMKSVDERKSFESSPILHEESKKRDIETTKSSQARPAVRSISLLSQFVYK GK BAJ43803.1 E.coli ExoI 58 >gi|315136644|dbj|BAJ43803.1| exonuclease I [Escherichia coli DH1] MMNDGKQQSTFLFHDYETFGTHPALDRPAQFAAIRTDSEFNVIGEPEVFYCKPADDYLPQPGAVLITGIT PQEARAKGENEAAFAARIHSLFTVPKTCILGYNNVRFDDEVTRNIFYRNFYDPYAWSWQHDNSRWDLLDV MRACYALRPEGINWPENDDGLPSFRLEHLTKANGIEHSNAHDAMADVYATIAMAKLVKTRQPRLFDYLFT HRNKHKLMALIDVPQMKPLVHVSGMFGAWRGNTSWVAPLAWHPENRNAVIMVDLAGDISPLLELDSDTLR ERLYTAKTDLGDNAAVPVKLVHINKCPVLAQANTLRPEDADRLGINRQHCLDNLKILRENPQVREKVVAI FAEAEPFTPSDNVDAQLYNGFFSDADRAAMKIVLETEPRNLPALDITFVDKRIEKLLFNYRARNFPGTLD YAEQQRWLEHRRQVFTPEFLQGYADELQMLVQQYADDKEKVALLKALWQYAEEIV Q913Q50.1 Human TREX2 59 >gi|47606206|sp|Q913Q50.1|TREX2_HUMAN RecName: Full = Three prime repair exonuclease 2; AltName: Full = 3′-5′ exonuclease TREX2 MGRAGSPLPRSSWPRMDDCGSRSRCSPTLCSSLRTCYPRGNITMSEAPRAETFVFLDLEATGLPSVEPEI AELSLFAVHRSSLENPEHDESGALVLPRVLDKLTLCMCPERPFTAKASEITGLSSEGLARCRKAGFDGAV VRTLQAFLSRQAGPICLVAHNGFDYDFPLLCAELRRLGARLPRDTVCLDTLPALRGLDRAHSHGTRARGR QGYSLGSLFHRYFRAEPSAAHSAEGDVHTLLLIFLHRAAELLAWADEQARGWAHIEPMYLPPDDPSLEA Q91XB0.2 Mouse TREX1 60 >gi|47606196|sp|Q91XB0.2|TREX1_MOUSE RecName: Full = Three prime repair exonuclease 1; AltName: Full = 3′-5′ exonuclease TREX1 MGSQTLPHGHMQTLIFLDLEATGLPSSRPEVTELCLLAVHRRALENTSISQGHPPPVPRPPRVVDKLSLC IAPGKACSPGASEITGLSKAELEVQGRQRFDDNLAILLRAFLQRQPQPCCLVAHNGDRYDFPLLQTELAR LSTPSPLDGTFCVDSIAALKALEQASSPSGNGSRKSYSLGSIYTRLYWQAPTDSHTAEGDVLTLLSICQW KPQALLQWVDEHARPFSTVKPMYGTPATTGTTNLRPHAATATTPLATANGSPSNGRSRRPKSPPPEKVPE APSQEGLLAPLSLLTLLTLAIATLYGLFLASPGQ Q9NSU2.1 Human TREX1 61 >gi|47606216|sp|Q9NSU2.1|TREX1_HUMAN RecName: Full = Three prime repair exonuclease 1; AltName: Full = 3′-5′ exonuclease TREX1; AltName: Full = DNase III MGPGARRQGRIVQGRPEMCFCPPPTPLPPLRILTLGTHTPTPCSSPGSAAGTYPTMGSQALPPGPMQTLI FEDMEATGLPFSQPKVTELCLLAVHRCALESPPTSQGPPPTVPPPPRVVDKLSLCVAPGKACSPAASEIT GLSTAVLAAHGRQCFDDNLANLLLAFLRRQPQPWCLVAHNGDRYDFPLLQAELAMLGLTSALDGAFCVDS ITALKALERASSPSEHGPRKSYSLGSIYTRLYGQSPPDSHTAEGDVLALLSICQWRPQALLRWVDAHARP FGTIRPMYGVTASARTKPRPSAVTTTAHLATTRNTSPSLGESRGTKDLPPVKDPGALSREGLLAPLGLLA ILTLAVATLYGLSLATPGE Q9BG99.1 Bovine TREX1 62 >gi|47606205|sp|Q9BG99.1|TREX1_BOVIN RecName: Full = Three prime repair exonuclease 1; AltName: Full = 3′-5′ exonuclease TREX1 MGSRALPPGPVQTLIFLDLEATGLPFSQPKITELCLLAVHRYALEGLSAPQGPSPTAPVPPRVLDKLSLC VAPGKVCSPAASEITGLSTAVLAAHGRRAFDADLVNLIRTFLQRQPQPWCLVAHNGDRYDFPLLRAELAL LGLASALDDAFCVDSIAALKALEPTGSSSEHGPRKSYSLGSVYTRLYGQAPPDSHTAEGDVLALLSVCQW RPRALLRWVDAHAKPFSTVKPMYVITTSTGTNPRPSAVTATVPLARASDTGPNLRGDRSPKPAPSPKMCP GAPPGEGLLAPLGLLAFLTLAVAMLYGLSLAMPGQ AAH91242.1 Rat TREX1 63 >gi|60688197|gb|AAH91242.1| Trex1 protein [Rattus norvegicus] MGSQALPHGHMQTLIFLDLEATGLPYSQPKITELCLLAVHRHALENSSMSEGQPPPVPKPPRVVDKLSLC IAPGKPCSSGASEITGLTTAGLEAHGRQRFNDNLATLLQVFLQRQPQPCCLVAHNGDRYDEPLLQAELAS LSVISPLDGTFCVDSIAALKTLEQASSPSEHGPRKSYSLGSIYTRLYGQAPTDSHTAEGDVLALLSICQW KPQALLQWVDKHARPFSTIKPMYGMAATTGTASPRLCAATTSSPLATANLSPSNGRSRGKRPTSPPPENV PEAPSREGLLAPLGLLTFLTLAIAVLYGIFLASPGQ AAH63664.1 Human DNA2 64 >gi|39793966|gb|AAH63664.1| DNA2 protein [Homo sapiens] FAIPASRMEQLNELELLMEKSFWEEAELPAELFQKKVVASFPRTVLSTGMDNRYLVLAVNTVQNKEGNCE KRLVITASQSLENKELCILRNDWCSVPVEPGDIIHLEGDCTSDTWIIDKDFGYLILYPDMLISGTSIASS IRCMRRAVLSETFRSSDPATRQMLIGTVLHEVFQKAINNSFAPEKLQELAFQTIQEIRHLKEMYRLNLSQ DEIKQEVEDYLPSFCKWAGDFMHKNTSTDFPQMQLSLPSDNSKDNSTCNIEVVKPMDIEESIWSPRFGLK GKIDVTVGVKIHRGYKTKYKIMPLELKTGKESNSIEHRSQVVLYTLLSQERRADPEAGLLLYLKTGQMYP VPANHLDKRELLKLRNQMAFSLFHRISKSATRQKTQLASLPQIIEEEKTCKYCSQIGNCALYSRAVEQQM DCSSVPIVMLPKIEEETQHLKQTHLEYFSLWCLMLTLESQSKDNKKNHQNIWLMPASEMEKSGSCIGNLI RMEHVKIVCDGQYLHNFQCKHGAIPVTNLMAGDRVIVSGEERSLFALSRGYVKEINMTTVTCLLDRNLSV LPESTLFRLDQEEKNCDIDTPLGNLSKLMENTFVSKKLRDLIIDFREPQFISYLSSVLPHDAKDTVACIL KGLNKPQRQAMKKVLLSKDYTLIVGMPGTGKTTTICTLVPAPEQVEKGGVSNVTEAKLIVELTSIFVKAG CSPSDIGIIAPYRQQLKIINDLLARSIGMVEVNTVDKYQGRDKSIVLVSFVRSNKDGTVGELLKDWRRLN VAITRAKHKLILLGCVPSLNCYPPLEKLLNHLNSEKLIIDLPSREHESLCHILGDFQRE P38859.1 Yeast DNA2 65 >gi|731738|sp|P38859.1|DNA2_YEAST RecName: Full = DNA replication ATP- (DNA2_YEAST) dependent helicase DNA2 MPGTPQKNKRSASISVSPAKKTEEKEIIQNDSKAILSKQTKRKKKYAFAPINNLNGKNTKVSNASVLKSI AVSQVRNTSRTKDINKAVSKSVKQLPNSQVKPKREMSNLSRHHDFTQDEDGPMEEVIWKYSPLQRDMSDK TTSAAEYSDDYEDVQNPSSTPIVPNRLKTVLSFTNIQVPNADVNQLIQENGNEQVRPKPAEISTRESLRN IDDILDDIEGDLTIKPTITKFSDLPSSPIKAPNVEKKAEVNAEEVDKMDSTGDSNDGDDSLIDILTQKYV EKRKSESQITIQGNTNQKSGAQESCGKNDNTKSRGEIEDHENVDNQAKTGNAFYENEEDSNCQRIKKNEK IEYNSSDEFSDDSLIELLNETQTQVEPNTIEQDLDKVEKMVSDDLRIATDSTLSAYALRAKSGAPRDGVV RLVIVSLRSVELPKIGTQKILECIDGKGEQSSVVVREPWVYLEFEVGDVIHIIEGKNIENKRLLSDDKNP KTQLANDNLLVLNPDVLFSATSVGSSVGCLRRSILQMQFQDPRGEPSLVMTLGNIVHELLQDSIKYKLSH NKISMEIIIQKLDSLLETYSFSIIICNEEIQYVKELVMKEHAENILYFVNKFVSKSNYGCYTSISGTRRT QPISISNVIDIEENIWSPIYGLKGFLDATVEANVENNKKHIVPLEVKTGKSRSVSYEVQGLIYTLLLNDR YEIPIEFFLLYFTRDKNMTKFPSVLHSIKHILMSRNRMSMNFKHQLQEVFGQAQSRFELPPLLRDSSCDS CFIKESCMVLNKLLEDGTPEESGLVEGEFEILTNHLSQNLANYKEFFTKYNDLITKEESSITCVNKELFL LDGSTRESRSGRCLSGLVVSEVVEHEKTEGAYIYCFSRRANDNNSQSMLSSQIAANDEVIISDEEGHFCL CQGRVQFINPAKIGISVKRKLLNNRLLDKEKGVTTIQSVVESELEQSSLIATQNLVTYRIDKNDIQQSLS LARFNLLSLFLPAVSPGVDIVDERSKLCRKTKRSDGGNEILRSLLVDNRAPKFRDANDDPVIPYKLSKDT TLNLNQKEAIDKVMRAEDYALILGMPGTGKTTVIAEIIKILVSEGKRVLLTSYTHSAVDNILIKLRNTNI SIMRLGMKHKVHPDTQKYVPNYASVKSYNDYLSKINSTSVVATTCLGINDILFTLNEKDFDYVILDEASQ ISMPVALGPLRYGNRFIMVGDHYQLPPLVKNDAARLGGLEESLFKTFCEKHPESVAELTLQYRMCGDIVT LSNFLIYDNKLKCGNNEVFAQSLELPMPEALSRYRNESANSKQWLEDILEPTRKVVFLNYDNCPDIIEQS EKDNITNHGEAELTLQCVEGMLLSGVPCEDIGVMTLYRAQLRLLKKIFNKNVYDGLEILTADQFQGRDKK CIIISMVRRNSQLNGGALLKELRRVNVAMTRAKSKLIIIGSKSTIGSVPEIKSFVNLLEERNWVYTMCKD ALYKYKFPDRSNAIDEARKGCGKRTGAKPITSKSKFVSDKPIIKEILQEYES AAA45863.1 VP16 66 >gi|330318|gb|AAA45863.1| VP16 [Human herpesvirus 2] MDLLVDDLFADRDGVSPPPPRPAGGPKNTPAAPPLYATGRLSQAQLMPSPPMPVPPAALFNRLLDDLGFS AGPALCTMLDTWNEDLFSGFPTNADMYRECKFLSTLPSDVIDWGDAHVPERSPIDIRAHGDVAFPTLPAT RDELPSYYEAMAQFFRGELRAREESYRTVLANFCSALYRYLRASVRQLHRQAHMRGRNRDLREMLRTTIA DRYYRETARLARVLFLHLYLFLSREILWAAYAEQMMRPDLFDGLCCDLESWRQLACLFQPLMFINGSLTV RGVPVEARRLRELNHIREHLNLPLVRSAAAEEPGAPLTTPPVLQGNQARSSGYFMLLIRAKLDSYSSVAT SEGESVMREHAYSRGRTRNNYGSTIEGLLDLPDDDDAPAEAGLVAPRMSFLSAGQRPRRLSTTAPITDVS LGDELRLDGEEVDMTPADALDDFDLEMLGDVESPSPGMTHDPVSYGALDVDDFEFEQMFTDAMGIDDFGG ACM07430.1 Colicin E9 366 >gi|221185856|gb|ACM07430.1| colicin E9 [Escherichia coli] MSGGDGRGHNTGAHSTSGNINGGPTGIGVSGGASDGSGWSSENNPWGGGSGSGIHWGGGSGRGNGGGNGN SGGGSGTGGNLSAVAAPVAFGFPALSTPGAGGLAVSISASELSAAIAGIIAKLKKVNLKFTPFGVVLSSL IPSEIAKDDPNMMSKIVTSLPADDITESPVSSLPLDKATVNVNVRVVDDVKDERQNISVVSGVPMSVPVV DAKPTERPGVFTASIPGAPVLNISVNDSTPAVQTLSPGVTNNTDKDVRPAGFTQGGNTRDAVIRFPKDSG HNAVYVSVSDVLSPDQVKQRQDEENRRQQEWDATHPVEAAERNYERARAELNQANEDVARNQERQAKAVQ VYNSRKSELDAANKTLADAIAEIKQFNRFAHDPMAGGHRMWQMAGLKAQRAQTDVNNKQAAFDAAAKEKS DADAALSAAQERRKQKENKEKDAKDKLDKESKRNKPGKATGKGKPVGDKWLDDAGKDSGAPIPDRIADKL RDKEEKSFDDFRKAVWEEVSKDPELSKNLNPSNKSSVSKGYSPFTPKNQQVGGRKVYELHHDKPISQGGE VYDMDNIRVTTPKRHIDIHRGK NP_775816.1 APFL 367 >gi|135233|sp|P14870.1|T2F1_PLAOK RecName: Full = Type-2 restriction enzyme FokI; Short = R.FokI; AltName: Full = Endonuclease FokI;  AltName: Full = Type II restriction enzyme FokI; AltName: Full = Type IIS restriction enzyme FokI MFLSMVSKIRTFGWVQNPGKFENLKRVVQVFDRNSKVHNEVKNIKIPTLVKESKIQKELVAIMNQHDLIY TYKELVGTGTSIRSEAPCDAIIQATIADQGNKKGYIDNWSSDGFLRWAHALGFIEYINKSDSFVITDVGL AYSKSADGSAIEKEILIEAISSYPPAIRILTLLEDGQHLTKFDLGKNLGFSGESGFTSLPEGILLDTLAN AMPKDKGEIRNNWEGSSDKYARMIGGWLDKLGLVKQGKKEFIIPTLGKPDNKEFISHAFKITGEGLKVLR RAKGSTKFTRVPKRVYWEMLATNLTDKEYVRTRRALILEILIKAGSLKIEQIQDNLKKLGFDEVIETIEN DIKGLINTGIFIEIKGRFYQLKDHILQFVIPNRGVTKQLVKSELEEKKSELRHKLKYVPHEYIELIEIAR NSTQDRILEMKVMEFFMKVYGYRGKHLGGSRKPDGAIYTVGSPIDYGVIVDTKAYSGGYNLPIGQADEMQ RYVEENQTRNKHINPNEWWKVYPSSVTEFKFLFVSGHFKGNYKAQLTRLNHITNCNGAVLSVEELLIGGE MIKAGTLTLEEVRRKFNNGEINF P14870.1 Fokl 368 >gi|221185857|gb|ACM07431.1| colicin E9 immunity protein [Escherichia coli] MELKHSISDYTEAEFLQLVTTICNADISSEEELVKLVTHFEEMTEHPSGSDLIYYPKEGDDDSPSGIVNT VKQWRAANGKSGFKQG

In another preferred embodiment according to the method of the present invention, the peptidic linker that can link said catalytic domain to the core TALE scaffold according to the method of the present invention can be selected from the group consisting of NFS1, NFS2, CFS1, RM2, BQY, QGPSG, LGPDGRKA, 1a8h_1, 1dnpA_1, 1d8cA_2, 1ckqA_3, 1sbp_1, 1ev7A_1, 1alo_3, 1amf_1, 1adjA_3, 1fcdC_1, 1a13_2, 1g3p_1, 1acc_3, 1ahjB_1, 1acc_1, 1af7_1, 1heiA_1, 1bia_2, 1igtB_1, 1nfkA_1, 1au7A_1, 1 bpoB_1, 1b0pA_2, 1c05A_2, 1gcb_1, 1bt3A_1, 1b3o8_2, 16vpA_6, 1dhx_1, 1b8aA_1 and 1qu6A_1, as listed in Table 3 (SEQ ID NO: 67 to SEQ ID NO: 104 and SEQ ID NO: 372 to SEQ ID NO: 415). In a more preferred embodiment, the peptidic linker that can link said catalytic domain to the core TALE scaffold according to the method of the present invention can be selected from the group consisting of NFS1 (SEQ ID NO: 98), NFS2 (SEQ ID NO: 99) and CFS1 (SEQ ID NO: 100). In the scope of the present invention is also encompassed the case where a peptidic linker is not needed to fuse a catalytical domain to the TALE scaffold in order to obtain a cTALEN according to the present invention.

TABLE 3 List of peptidic linkers that can be used in compact TALENs or enhanced compact TALENs. Amino SEQ ID Name (PDB) Acids Size Length Sequence NO 1a8h_1 285-287 3 6,636 NVG 67 1dnpA_1 130-133 4 7,422 DSVI 68 1d8cA_2 260-263 4 8,782 IVEA 69 1ckqA_3 169-172 4 9,91 LEGS 70 1sbp_1 93-96 4 10,718 YTST 71 1ev7A_1 169-173 5 11,461 LQENL 72 1alo_3 360-364 5 12,051 VGRQP 73 1amf_1 81-85 5 13,501 LGNSL 74 1adjA_3 323-328 6 14,835 LPEEKG 75 1fcdC_1 76-81 6 14,887 QTYQPA 76 1al3_2 265-270 6 15,485 FSHSTT 77 1g3p_1  99-105 7 17,903 GYTYINP 78 1acc_3 216-222 7 19,729 LTKYKSS 79 1ahjB_1 106-113 8 17,435 SRPSESEG 80 1acc_1 154-161 8 18,776 PELKQKSS 81 1af7_1 89-96 8 22,502 LTTNLTAF 82 1heiA_1 322-330 9 13,534 TATPPGSVT 83 1bia_2 268-276 9 16,089 LDNFINRPV 84 1igtB_1 111-119 9 19,737 VSSAKTTAP 85 1nfkA_1 239-248 10 13,228 DSKAPNASNL 86 1au7A_1 103-112 10 20,486 KRRTTISIAA 87 1bpoB_1 138-148 11 21,645 PVKMFDRHSSL 88 1b0pA_2 625-635 11 26,462 APAETKAEPMT 89 1c05A_2 135-148 14 23,819 YTRLPERSELPAEI 90 1gcb_1 57-70 14 27,39 VSTDSTPVTNQKSS 91 1bt3A_1 38-51 14 28,818 YKLPAVTTMKVRPA 92 1b3oB_2 222-236 15 20,054 IARTDLKKNRDYPLA 93 16vpA_6 312-332 21 23,713 TEEPGAPLTTPPTLHGNQARA 94 1dhx_1  81-101 21 42,703 ARFTLAVGDNRVLDMASTYFD 95 1b8aA_1  95-120 26 31,305 IVVLNRAETPLPLDPTGKVKAELDTR 96 1qu6A_1  79-106 28 51,301 ILNKEKKAVSPLLLTTTNSSEGLSMGNY 97 NFS1 — 20 — GSDITKSKISEKMKGQGPSG 98 NFS2 — 23 — GSDITKSKISEKMKGLGPDGRKA 99 CFS1 — 10 — SLTKSKISGS 100 RM2 — 32 — AAGGSALTAGALSLTAGALSLTAGALSGGGGS 101 BQY — 25 — AAGASSVSASGHIAPLSLPSSPPSVGS 102 QGPSG — 5 — QGPSG 103 LGPDGRKA — 8 — LGPDGRKA 104 TAL1 — 15 — SGGSGSNVGSGSGSG 372 TAL2 — 20 — SGGSGSLTTNLTAFSGSGSG 373 TAL3 — 22 — SGGSGSKRRTTISIAASGSGSG 374 TAL4 — 17 — SGGSGSVGRQPSGSGSG 375 TAL5 — 26 — SGGSGSYTRLPERSELPAEISGSGSG 376 TAL6 — 38 — SGGSGSIVVLNRAETPLPLDPTGKVKAELDTRSGSGSG 377 TAL7 — 21 — SGGSGSTATPPGSVTSGSGSG 378 TAL8 — 21 — SGGSGSLDNFINRPVSGSGSG 379 TAL9 — 21 — SGGSGSVSSAKTTAPSGSGSG 380 TAL10 — 22 — SGGSGSDSKAPNASNLSGSGSG 381 TAL11 — 23 — SGGSGSPVKMFDRHSSLSGSGSG 382 TAL12 — 23 — SGGSGSAPAETKAEPMTSGSGSG 383 TAL13 — 26 — SGGSGSVSTDSTPVTNQKSSSGSGSG 384 TAL14 — 16 — SGGSGSDSVISGSGSG 385 TAL15 — 33 — SGGSGSARFTLAVGDNRVLDMASTYFDSGSGSG 386 TAL16 — 17 — SGGSGSLQENLSGSGSG 387 TAL17 — 19 — SGGSGSGYTYINPSGSGSG 388 TAL18 — 26 — SGGSGSYKLPAVITMKVRPASGSGSG 389 TAL19 — 16 — SGGSGSLEGSSGSGSG 390 TAL20 — 16 — SGGSGSIVEASGSGSG 391 TAL21 — 18 — SGGSGSQTYQPASGSGSG 392 TAL22 — 27 — SGGSGSIARTDLKKNRDYPLASGSGSG 393 TAL23 — 18 — SGGSGSLPEEKGSGSGSG 394 TAL24 — 16 — SGGSGSYTSTSGSGSG 395 TAL25 — 20 — SGGSGSSRPSESEGSGSGSG 396 TAL26 — 17 — SGGSGSLGNSLSGSGSG 397 TAL27 — 19 — SGGSGSLTKYKSSSGSGSG 398 TAL28 — 33 — SGGSGSTEEPGAPLTTPPTLHGNQARASGSGSG 399 TAL29 — 18 — SGGSGSFSHSTTSGSGSG 400 TAL30 — 20 — SGGSGSPELKQKSSSGSGSG 401 TAL31 — 40 — SGGSGSILNKEKKAVSPLIITTINSSEGLSMGNYSGSGSG 402 TAL32 — 31 — ELAEFHARYADLLLRDLRERPVSLVRGPDSG 403 TAL33 — 31 — ELAEFHARPDPLLLRDLRERPVSLVRGLGSG 404 TAL34 — 26 — ELAEFHARYADLLLRDLRERSGSGSG 405 TAL35 — 31 — DIFDYYAGVAEVMLGHIAGRPATRKRWPNSG 406 TAL36 — 31 — DIFDYYAGPDPVMLGHIAGRPATRKRWLGSG 407 TAL37 — 26 — DIFDYYAGVAEVMLGHIAGRSGSGSG 408 Linker A 37 SIVAQLSRPDPALVSFQKLKLACLGGRPALDAVKKGL 409 Linker B 37 SIVAQLSRPDPAAVSAQKAKAACLGGRPALDAVKKGL 410 Linker C 37 SIVAQLSRPDPAVVTFHKLKLACLGGRPALDAVKKGL 411 Linker D 44 SIVAQLSRPDPAQSLAQELSLNESQIKIACLGGRPALDAVKKGL 412 Linker E 40 SIVAQLSRPDPALQLPPLERLTLDACLGGRPALDAVKKGL 413 Linker F 38 SIVAQLSRPDPAIHKKFSSIQMACLGGRPALDAVKKGL 414 Linker G 40 SIVAQLSRPDPAAAAATNDHAVAAACLGGRPALDAVKKGL 415

Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities and eventually type of linker(s)], a compact TALEN according to the present invention can comprise different levels of separate enzymatic activities able to differently process DNA, resulting in a global DNA processing efficiency for said compact TALEN, each one of said different enzymatic activities having their own DNA processing efficiency.

In another preferred embodiment, the method according to the present invention further comprises the steps of:

-   -   (i) Engineering at least one enhancer domain;     -   (ii) Optionally determining or engineering one peptide linker to         fuse said enhancer domain to one part of said compact TALEN         entity;         thereby obtaining a compact TALEN entity with enhanced DNA         processing efficiency nearby a single double-stranded DNA target         sequence of interest, i.e. an enhanced compact TALEN.

In other words, according to the method of the present invention said unique compact TALEN monomer further comprises:

-   -   (i) At least one enhancer domain;     -   (ii) Optionally one peptide linker to fuse said enhancer domain         to one part of said unique compact TALEN monomer active entity.

In another more preferred embodiment, said enhancer domain is fused to the N-terminus of the core TALE scaffold part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused to C-terminus of the core TALE scaffold part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused to the catalytic domain part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused between the N-terminus of the core TALE scaffold part and the catalytic part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused between the C-terminus of the core TALE scaffold part and the catalytic part of said compact TALEN entity. In the scope of the present invention, it can be envisioned to insert said catalytic domain and/or enhancer domain between two parts of the engineered core TALE scaffold according to the invention, each part comprising one set of RVDs. In this last case, the number of RVDs for each engineered core TALE scaffold can be the same or not. In other words, it can be envisioned to split said core TALE scaffold of the present invention to insert one catalytic domain and/or one enhancer domain between the resulting two parts of said engineered core TALE scaffold.

In another preferred embodiment, said enhancer domain is catalytically active or not, providing functional and/or structural support to said compact TALEN entity. In a more preferred embodiment, said enhancer domain consists of a protein domain selected from the group consisting of MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367, a functional mutant, a variant or a derivative thereof. In another more preferred embodiment, said enhancer domain consists of a catalytically active derivative of the protein domains listed above and in Table 2, providing functional and/or structural support to said compact TALEN entity. In another preferred embodiment, said enhancer domain consists of a catalytically inactive derivative of the protein domains listed above and in Table 2, providing structural support to said compact TALEN entity. In another preferred embodiment, said enhancer domain is selected from the group consisting of I-TevI (SEQ ID NO: 20), ColE7 (SEQ ID NO: 11) and NucA (SEQ ID NO: 26).

In a more preferred embodiment, said enhanced compact TALEN according to the method of the present invention can comprise a second enhancer domain. In this embodiment, said second enhancer domain can have the same characteristics than the first enhancer domain. In a more preferred embodiment, said second enhancer domain provides structural support to enhanced compact TALEN entity. In another more preferred embodiment, said second enhancer domain provides functional support to enhanced compact TALEN entity. In a more preferred embodiment, said second enhancer domain provides structural and functional support to the enhanced compact TALEN entity. In a more preferred embodiment, said enhanced compact TALEN entity comprises one catalytic domain and one enhancer domain. In another more preferred embodiment said enhanced compact TALEN entity comprises one catalytic domain and two enhancer domains. In another more preferred embodiment said enhanced compact TALEN entity comprises two catalytic domains and one enhancer domains. In another more preferred embodiment said enhanced compact TALEN entity comprises two catalytic domains and two enhancer domains.

In a more preferred embodiment, said second enhancer domain consists of a protein domain derived from a protein selected from the group consisting of MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AiwI, Mva12691, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367, a functional mutant, a variant or a derivative thereof. In another more preferred embodiment, said second enhancer domain consists of a catalytically active derivative of the protein domains listed above and in Table 2, providing functional and/or structural support to said enhanced compact TALEN entity. In another preferred embodiment, said second enhancer domain consists of a catalytically inactive derivative of the protein domains listed above and in Table 2, providing structural support to said enhanced compact TALEN entity.

In another more preferred embodiment, any combinations of catalytic and/or enhancer domains listed above, as non-limiting examples, can be envisioned to be fused to said core TALE scaffold providing structural and/or functional support to said compact TALEN entity. More preferably, combinations of catalytic domains selected from the group of TevI (SEQ ID NO: 20), ColE7 (SEQ ID NO: 11) and NucA (SEQ ID NO: 26) can be envisioned. Optionally, FokI (SEQ ID NO: 368) can be used in combination with another catalytic domain according to the list of Tablet. Such combinations of catalytic and/or enhancer domains can be envisioned regarding the envisioned applications for using the method of the present invention.

Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities, eventually type of linker(s) and type of enhancer(s) domains], an enhanced compact TALEN according to the present invention can present different levels of separate enzymatic activities able to differently process DNA, resulting in a global DNA processing efficiency for said enhanced compact TALEN, each one of said different enzymatic activities having their own DNA processing efficiency.

In this preferred embodiment, the DNA processing efficiency of the compact TALEN entity according to the method of the present invention can be enhanced by the engineering of at least one enhancer domain and one peptidic linker thereby obtaining a compact TALEN entity with enhanced DNA processing activity nearby a single double-stranded DNA target sequence of interest, i.e. a enhanced compact TALEN according to the present invention.

Depending on its structural composition, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention, can have a dominant enzymatic activity selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In a more preferred embodiment, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention is a combination of different enzymatic activities selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In a more preferred embodiment, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention is one of its different enzymatic activities selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In this case, the global DNA processing efficiency is equivalent to one DNA processing activity amongst the enzymatic activities mentioned above. In another more preferred embodiment, said DNA processing activity of the compact TALEN entity which is enhanced by the enhancer is a cleavase activity or a nickase activity or a combination of both a cleavase activity and a nickase activity.

Enhancement of DNA processing efficiency of a compact TALEN entity according to the present invention can be a consequence of a structural support by at least one enhancer domain. In a preferred embodiment, said structural support enhances the binding of a compact TALEN entity according to the invention for said DNA target sequence compared to the binding of a starting compact TALEN entity for the same DNA target sequence, thereby indirectly assisting the catalytic domain(s) to obtain a compact TALEN entity with enhanced DNA processing activity. In another preferred embodiment, said structural support enhances the existing catalytical activity of a compact TALEN entity for a DNA target sequence compared to the binding of a starting compact TALEN entity for the same DNA target sequence to obtain a compact TALEN entity with enhanced DNA processing activity.

In another preferred embodiment, said enhancer according to the method of the present invention both enhances the binding of the compact TALEN entity for said DNA target sequence and the catalytic activity of the catalytic domain(s) to obtain a compact TALEN entity with enhanced DNA processing activity. All these non-limiting examples lead to a compact TALEN entity with enhanced DNA processing efficiency for a DNA target sequence at a genomic locus of interest, i.e. an enhanced compact TALEN according to the present invention.

Enhancement of DNA processing efficiency of a compact TALEN entity according to the present invention, compared to a starting compact TALEN entity, can also be a consequence of a fuctional support by at least one enhancer domain. In a preferred embodiment, said functional support can be the consequence of the hydrolysis of additional phosphodiester bonds. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a nuclease. In an embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from an endonuclease. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a cleavase. In another more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a nickase. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from an exonuclease.

In genome engineering experiments, the efficiency of rare-cutting endonuclease, e.g. their ability to induce a desired event (Homologous gene targeting, targeted mutagenesis, sequence removal or excision) at a locus, depends on several parameters, including the specific activity of the nuclease, probably the accessibility of the target, and the efficacy and outcome of the repair pathway(s) resulting in the desired event (homologous repair for gene targeting, NHEJ pathways for targeted mutagenesis).

Cleavage by peptidic rare cutting endonucleases usually generates cohesive ends, with 3′ overhangs for LAGLIDADG meganucleases (Chevalier and Stoddard 2001) and 5′ overhangs for Zinc Finger Nucleases (Smith, Bibikova et al. 2000). These ends, which result from hydrolysis of phosphodiester bonds, can be re-ligated in vivo by NHEJ in a seamless way (i.e. a scarless re-ligation). The restoration of a cleavable target sequence allows for a new cleavage event by the same endonuclease, and thus, a series of futile cycles of cleavage and re-ligation events can take place. Indirect evidences have shown that even in the yeast Saccharomyces cerevisiae, such cycles could take place upon continuous cleavage by the HO endonuclease (Lee, Paques et al. 1999). In mammalian cells, several experiment have shown that perfect re-ligation of compatible cohesive ends resulting from two independent but close I-SceI-induced DSBs is an efficient process (Guirouilh-Barbat, Huck et al. 2004; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Cheng et al. 2008; Bennardo, Gunn et al. 2009). Absence of the Ku DNA repair protein does not significantly affect the overall frequency of NHEJ events rejoining the ends from the two DSBs; however it very strongly enhances the contribution of imprecise NHEJ to the repair process in CHO immortalized cells and mouse ES cells (Guirouilh-Barbat, Huck et al. 2004; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Cheng et al. 2008). Furthermore, the absence of Ku stimulates I-SceI-induced events such as imprecise NHEJ (Bennardo, Cheng et al. 2008), single-strand annealing (Bennardo, Cheng et al. 2008) and gene conversion (Pierce, Hu et al. 2001; Bennardo, Cheng et al. 2008) in mouse ES cells. Similar observations shave been made with cells deficient for the XRCC4 repair protein (Pierce, Hu et al. 2001; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Gunn et al. 2009) (although XRCC4 deficiency affects the overal level of NHEJ in CHO cells (Guirouilh-Barbat, Rass et al. 2007)) or for DNA-PK (Pierce, Hu et al. 2001). In contrast, knock-down of CtIP has been shown to suppresses “alt-NHEJ” (a Ku- and XRCC4-independent form of NHEJ more prone to result in imprecise NHEJ), single-strand annealing and gene conversion, while not affecting the overall level of rejoining of two compatible ends generated by I-SceI (Bennardo, Cheng et al. 2008). Thus, competition between different DSB repair pathways can affect the spectrum or repair events resulting from a nuclease-induced DSB.

In addition, DSB resection is important for certain DSB pathways. Extensive DSB resection, resulting in the generation of large single stranded regions (a few hundred nucleotides at least), has been shown in yeast to initiate single strand annealing (Sugawara and Haber 1992) and strand invasion, the ATP-dependant step that initiates many homologous recombination events of DNA duplex invasion by an homologous strand that (White and Haber 1990; Sun, Treco et al. 1991) (for a review of mechanisms, see (Paques and Haber 1999)). In eukaryotic cells DSB resection depends on several proteins including BLM/Sgs1 and DNA2, EXOI, and the MRN complex (Mre11, Rad50, Nbs1/Xrs2) and is thought to result from different pathways. MRN is involved in a small scale resection process, while two redundant pathways depending on BLM and DNA2 on one hand, and on EXOI on another hand, would be involved in extensive resection (Mimitou and Symington 2008; Nimonkar, Genschel et al. 2011). In addition, processing ends involving a damaged nucleotide (resulting from chemical cleavage or from a bulk adduct), requires the CtlP/Sae2 protein together with RMN (Sartori, Lukas et al. 2007; Buis, Wu et al. 2008; Hartsuiker, Mizuno et al. 2009). Over-expression of the Trex2 exonuclease was shown to strongly stimulate imperfect NHEJ associated with loss of only a few base pairs (Bennardo, Gunn et al. 2009), while it inhibited various kinds of DNA repair events between distant sequences (such as Single-strand annealing, NHEJ between ends from different breaks, or NHEJ repair of a single DSB involving remote micro-homologies). In the same study, it was suggested that Trex2 did resect the 3′ overhangs let by I-SceI in a non processive way. Thus, the type of stimulated pathway could in turn depend on the type of resection (length of resection, single strand vs. double strand, resection of 5′ strand vs. 3′ strand).

Thus, the efficiency of a compact TALEN, e.g. it ability to produce a desired event such as targeted mutagenesis or homologous gene targeting (see definition for full definition of “efficiency of compact TALEN”), can be enhanced by an enhancement or modification of its global DNA processing efficiency (see definition for full definition of “global DNA processing efficiency”), e.g. the global resultant or the overall result of different separate enzymatic activities that said compact TALEN.

In a preferred embodiment, enhancement of global DNA processing efficiency of a compact TALEN entity according to the present invention, compared to a starting compact TALEN entity, can be the hydrolysis of additional phosphodiester bonds at the cleavage site.

Said hydrolysis of additional phosphodiester bonds at the cleavage site by said at least one enhancer according to the invention can lead to different types of DSB resection affecting at said DSB cleavage site, one single DNA strand or both DNA strands, affecting either 5′ overhangs ends, either 3′ overhangs ends, or both ends and depending on the length of said resection. Thus, adding new nickase or cleavase activities to the existing cleavase activity of a compact TALEN entity can enhance the efficiency of the resulting enhanced compact TALEN according to the invention, at a genomic locus of interest (FIG. 8B-8E). As a non-limiting example, addition of two nickase activities on opposite strands (FIG. 8D) or of a new cleavase activity generating a second DSB (FIG. 8E) can result in a double-strand gap. As a consequence, perfect religation is no longer possible, and one or several alternative repair outcomes such as imprecise NHEJ, Homologous Recombination or SSA for instance, can be stimulated. As another non-limiting example, the addition of a single nickase activity can result in a single strand gap, and suppress the cohesiveness of the ends, which can also enhance the efficiency of the resulting enhanced compact TALEN at a genomic locus of interest, according to the invention, via stimulation of one or several alternative repair outcomes mentioned above.

In this aspect of the present invention, enhancement of DNA processing efficiency of a compact TALEN refers to the increase in the detected level of said DNA processing efficiency, against a target DNA sequence, of a enhanced compact TALEN in comparison to the activity of a first compact TALEN against the same target DNA sequence. Said first compact TALEN can be a starting compact TALEN, or a compact TALEN that has already been engineered or an enhanced compact TALEN according to the present invention. Several rounds of enhancement can be envisioned from a starting compact TALEN or from a starting enhanced compact TALEN.

In this aspect of the method of the present invention, enhancement of the DNA processing efficiency of the compact TALEN entity (or enhanced compact TALEN) refers to the increase in the detected level of said DNA processing efficiency against a target DNA sequence of interest or nearby said DNA sequence of interest in comparison to the efficiency of a first compact TALEN or starting compact TALEN against or nearby the same target DNA sequence. In this case, the starting compact TALEN is taken as the reference scaffold to measure the DNA processing efficiency. Said enhanced compact TALEN is an engineered compact TALEN comprising an enhancer domain according to this aspect of the invention. Said enhanced compact TALEN can also be taken as a reference scaffold for further enhancement of said DNA processing efficiency. As a non-limiting example, said DNA processing efficiency can result from a cleavage-induced recombination generated by said enhanced compact TALEN. In this case, said level of cleavage-induced recombination can be determined, for instance, by a cell-based recombination assay as described in the International PCT Application WO 2004/067736. Importantly, enhancement of efficacy in cells (enhanced generation of targeted mutagenesis or targeted recombination) can be, but is not necessarily associated with an enhancement of the cleavage activity that could be detected in certain in vitro assays. For example, additional phosphodiesterase activities as described in FIG. 8 could barely affect the cleavage profile, as detected by in vitro cleavage and separation of the cleavage products on an electrophoresis gel. However, as explained above, and in the legend of FIG. 8, the DSB ends generated in this way could be more prone to induce detectable genomic rearrangements such as targeted mutagenesis (by imprecise NHEJ) or homologous recombination. Said enhancement in cleavage-induced recombination of said enhanced compact TALEN is at least a 5% enhancement compared to the starting scaffold or starting compact TALEN, more preferably at least a 10% enhancement, again more preferably at least a 15% enhancement, again more preferably at least a 20% enhancement, again more preferably at least a 25% enhancement, again more preferably a 50% enhancement, again more preferably an enhancement greater than 50%, resulting in an enhancement of DNA processing efficiency of said enhanced compact TALEN of at least 5% compared to the starting scaffold or starting compact TALEN, more preferably at least a 10% enhancement, again more preferably at least a 15% enhancement, again more preferably at least a 20% enhancement, again more preferably at least a 25% enhancement, again more preferably a 50% enhancement, again more preferably a enhancement greater than 50%.

In another preferred embodiment according to the method of the present invention, the peptidic linker that can link said enhancer domain to one part of said compact TALEN entity according to the method of the present invention can be selected from the group consisting of NFS1, NFS2, CFS1, RM2, BQY, QGPSG (SEQ ID NO: 469), LGPDGRKA (SEQ ID NO: 104), 1a8h_1, 1dnpA_1, 1d8cA_2, 1ckqA_3, 1sbp_1, 1ev7A_1, 1alo_3, 1amf_1, 1adjA_3, 1fcdC 1, 1a13_2, 1g3p_1, 1acc_3, 1ahjB_1, 1acc_1, 1af7_1, 1heiA_1, 1bia_2, 1igtB_1, 1nfkA_1, 1au7A_1, 1bpoB_1, 1b0 pA_2, 1c05A_2, 1gcb_1, 1bt3A_1, 1b3o13_2, 16vpA_6, 1dhx_1, 1b8aA_1 and 1qu6A_1 as listed in Table 3 (SEQ ID NO: 67 to SEQ ID NO: 104 and SEQ ID NO: 372 to SEQ ID NO: 415). In a more preferred embodiment, the peptidic linker that can said enhancer domain to one part of said compact TALEN entity according to the method of the present invention can be selected from the group consisting of NFS1 (SEQ ID NO: 98), NFS2 (SEQ ID NO: 99) and CFS1 (SEQ ID NO: 100). In the scope of the present invention is also encompassed the case where a peptidic linker is not needed to fuse one enhancer domain to one part of said compact TALEN entity in order to obtain a enhanced compact TALEN according to the present invention.

Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities, type of enhancers and eventually type of linker(s)], a compact TALEN or an enhanced compact TALEN according to the present invention can comprise different levels of separate enzymatic activities able to differently process DNA as mentioned above. By adding new enzymatic activities to said compact TALEN or said enhanced compact TALEN or enhancing the DNA processing efficiency of one or several of its constitutive enzymatic activities, one can enhance the global DNA processing efficiency of one compact TALEN or enhanced compact TALEN in comparison to a starting compact TALEN or enhanced compact TALEN.

According to the present invention, compact TALENs are designed to alleviate the need for multiple independent protein moieties when targeting a DNA processing event. Importantly, the requisite “spacer” region and dual target sites essential for the function of current TALENs are unnecessary. As each end of the core TALE scaffold is amenable to fusion, the order (N- v.s C-terminal) of addition of the catalytic and enhancement domains can vary with the application. In addition, since the catalytic domain does not require specific DNA contacts, there are no restrictions on regions surrounding the core TALE scaffold, as non-limiting examples depicted in FIG. 5: (A) N-terminal fusion construct to promote Homologous recombination induced by a cleavase domain or by a nickase domain. (B) C-terminal fusion construct with properties as in (A). (C) The attachment of two catalytic domains to both ends of the core TALE scaffold allows for dual cleavage with enhancement in NHEJ. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application.

According to the present invention, compact TALENs can be enhanced through the addition of a domain to promote existing or alternate activities as non-limiting examples depicted in FIG. 6: (A) A standard compact TALEN with an enhancer domain fused to the C-terminus of its core TALE scaffold part. (B) The enhancer domain is fused to the compact TALEN via the N-terminus of its catalytic domain part. Such a configuration can be used to assist and/or anchor the catalytic domain part near the DNA to increase DNA processing activity. (C) The enhancer domain is sandwiched between the catalytic domain part and the core TALE scaffold part. The enhancer domain can promote communication between the flanking domains (i.e. to assist in catalysis and/or DNA binding) or can be used to overcome the requisite T nucleotide at position −1 of all TALE-based targets. (D) The enhancer domain is used to functionally replace the engineered core TALE scaffold N-terminal region. (E) The enhancer domain is used to functionally replace the engineered core TALE scaffold C-terminal region. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application.

According to the present invention, the nature of the catalytic domain(s) comprised in the compact TALEN and the enhanced compact TALEN is application dependent. As a non-limiting example, a nickase domain should allow for a higher HR/NHEJ ratio than a cleavase domain, thereby being more agreeable for therapeutic applications (McConnell Smith, Takeuchi et al. 2009; Metzger, McConnell-Smith et al. 2011). For example, the coupling of a cleavase domain on one side with a nickase domain on the other could result in excision of a single-strand of DNA spanning the binding region of a compact TALEN. The targeted generation of extended single-strand overhangs could be applied in applications that target DNA repair mechanisms. For targeted gene inactivation, the use of two cleavase domains is then preferred. In another preferred embodiment, the use of two nickase domains can be favored. Furthermore, the invention relates to a method for generating several distinct types of compact TALENs that can be applied to applications ranging from targeted DNA cleavage to targeted gene regulation.

In another aspect, the present invention relates to a compact TALEN comprising:

-   -   (i) One core TALE scaffold comprising different sets of Repeat         Variable Dipeptide regions (RVDs) to change DNA binding         specificity and target a specific single double-stranded DNA         target sequence of interest, onto which a selection of catalytic         domains can be attached to effect DNA processing;     -   (ii) At least one catalytic domain wherein said catalytic domain         is capable of processing DNA nearby said single double-stranded         DNA target sequence of interest when fused to said engineered         core TALE scaffold from (i);     -   (iii) Optionally one peptidic linker to fuse said catalytic         domain from (ii) to said engineered core TALE scaffold from (i)         when needed;         such that said compact TALEN does not require dimerization to         target a specific single double-stranded DNA target sequence of         interest and process DNA nearby said single double-stranded DNA         target sequence of interest. In other words, the compact TALEN         according to the present invention is an active entity unit         able, by itself, to target only one specific single         double-stranded DNA target sequence of interest through one DNA         binding domain and to process DNA nearby said single         double-stranded DNA target sequence of interest.

The present invention relates to a compact TALEN monomer comprising:

-   -   (i) One core TALE scaffold comprising Repeat Variable Dipeptide         regions (RVDs) having DNA binding specificity onto a specific         double-stranded DNA target sequence of interest;     -   (ii) At least one catalytic domain wherein said catalytic domain         is capable of processing DNA a few base pairs away from said         double-stranded DNA target sequence of interest when fused to         the C or N terminal of said core TALE scaffold from (i);     -   (iii) Optionally one peptidic linker to fuse said catalytic         domain from (ii) to said engineered core TALE scaffold from (i)         when needed;         wherein said compact TALEN monomer is assembled to bind said         target DNA sequence and process double-stranded DNA without         requiring dimerization.

In another embodiment, said engineered core TALE scaffold of the compact TALEN according to the present invention comprises an additional N-terminal domain resulting in an engineered core TALE scaffold sequentially comprising a N-terminal domain and different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest, onto which a selection of catalytic domains can be attached to effect DNA processing.

In another embodiment, said engineered core TALE scaffold of the compact TALEN according to the present invention comprises an additional C-terminal domain resulting in an engineered core TALE scaffold sequentially comprising different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest and a C-terminal domain, onto which a selection of catalytic domains can be attached to effect DNA processing.

In another embodiment, said engineered core TALE-scaffold of the compact TALEN according to the present invention comprises additional N-terminus and a C-terminal domains resulting in an engineered core TALE scaffold sequentially comprising a N-terminal domain, different sets of Repeat Variable Dipeptide regions (RVDs) to change DNA binding specificity and target a specific single double-stranded DNA target sequence of interest and a C-terminal domain, onto which a selection of catalytic domains can be attached to effect DNA processing.

In another embodiment, said engineered core TALE-scaffold according to the present invention comprises the protein sequences selected from the group consisting of ST1 (SEQ ID NO: 134) and ST2 (SEQ ID NO: 135). In another embodiment, said engineered core TALE scaffold comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 134 and SEQ ID NO: 135. In another embodiment, said engineered core TALE-scaffold according to the present invention comprises the protein sequences selected from the group consisting of bT1-Avr (SEQ ID NO: 136), bT2-Avr (SEQ ID NO: 137), bT1-Pth (SEQ ID NO: 138) and bT2-Pth (SEQ ID NO: 139). In another embodiment, said engineered TALE-scaffold comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 136 to SEQ ID NO: 139.

In a preferred embodiment, said additional N-terminus and C-terminal domains of engineered core TALE scaffold are derived from natural TALE. In a more preferred embodiment said additional N-terminus and C-terminal domains of engineered core TALE scaffold are derived from natural TALE selected from the group consisting of AvrBs3, PthXo1, AvrHah1, PthA, Tal1c as non-limiting examples. In another more preferred embodiment, said additional N-terminus and/or said C-terminal domains are truncated forms of respective N-terminus and/or said C-terminal domains of natural TALE like AvrBs3, PthXo1, AvrHah1, PthA, Tal1c as non-limiting examples, from which they are derived. In a more preferred embodiment, said additional N-terminus and C-terminal domains sequences of engineered core TALE scaffold are selected from the group consisting of ST1 SEQ ID NO: 134 and ST2 SEQ ID NO: 135 as respectively exemplified in baseline protein scaffolds bT1-Avr (SEQ ID NO: 136) or bT1-Pth (SEQ ID NO: 138) and bT2-Avr (SEQ ID NO: 137) or bT2-Pth (SEQ ID NO: 139).

In another embodiment, each RVD of said core scaffold is made of 30 to 42 amino acids, more preferably 33 or 34 wherein two critical amino acids located at positions 12 and 13 mediates the recognition of one nucleotide of said nucleic acid target sequence; equivalent two critical amino acids can be located at positions other than 12 and 13 specialy in RVDs taller than 33 or 34 amino acids long. Preferably, RVDs associated with recognition of the different nucleotides are HD for recognizing C, NG for recognizing T, NI for recognizing A, NN for recognizing G or A, NS for recognizing A, C, G or T, HG for recognizing T, IG for recognizing T, NK for recognizing G, HA for recognizing C, ND for recognizing C, HI for recognizing C, HN for recognizing G, NA for recognizing G, SN for recognizing G or A and YG for recognizing T, TL for recognizing A, VT for recognizing A or G and SW for recognizing A. More preferably, RVDs associated with recognition of the nucleotides C, T, A, G/A and G respectively are selected from the group consisting of NN or NK for recognizing G, HD for recognizing C, NG for recognizing T and NI for recognizing A, TL for recognizing A, VT for recognizing A or G and SW for recognizing A. In another embodiment, RVDS associated with recognition of the nucleotide C are selected from the group consisting of N* and RVDS associated with recognition of the nucleotide T are selected from the group consisting of N* and H*, where * denotes a gap in the repeat sequence that corresponds to a lack of amino acid residue at the second position of the RVD. In another embodiment, critical amino acids 12 and 13 can be mutated towards other amino acid residues in order to modulate their specificity towards nucleotides A, T, C and G and in particular to enhance this specificity. By other amino acid residues is intended any of the twenty natural amino acid residues or unnatural amino acids derivatives.

In another embodiment, said core scaffold of the present invention comprises between 8 and 30 RVDs. More preferably, said core scaffold of the present invention comprises between 8 and 20 RVDs; again more preferably 15 RVDs.

In another embodiment, said core scaffold comprises an additional single truncated RVD made of 20 amino acids located at the C-terminus of said set of RVDs, i.e. an additional C-terminal half-RVD. In this case, said core scaffold of the present invention comprises between 8.5 and 30.5 RVDs, “0.5” referring to previously mentioned half-RVD (or terminal RVD, or half-repeat). More preferably, said core scaffold of the present invention comprises between 8.5 and 20.5 RVDs, again more preferably, 15.5 RVDs. In a preferred embodiment, said half-RVD is in a core scaffold context which allows a lack of specificity of said half-RVD toward nucleotides A, C, G, T. In a more preferred embodiment, said half-RVD is absent.

In another embodiment, said core scaffold of the present invention comprises RVDs of different origins. In a preferred embodiment, said core scaffold comprises RVDs originating from different naturally occurring TAL effectors. In another preferred embodiment, internal structure of some RVDs of the core scaffold of the present invention are constituted by structures or sequences originated from different naturally occurring TAL effectors. In another embodiment, said core scaffold of the present invention comprises RVDs-like domains. RVDs-like domains have a sequence different from naturally occurring RVDs but have the same function and/or global structure within said core scaffold of the present invention.

In another embodiment, said additional N-terminal domain of said engineered core TALE scaffold of said compact TALEN according to the present invention is an enhancer domain. In another embodiment, said enhancer domain is selected from the group consisting of Puf RNA binding protein or Ankyrin super-family, as non-limiting examples. In another embodiment, said enhancer domain sequence is selected from the group consisting of protein domains of SEQ ID NO: 4 and SEQ ID NO: 5 as non-limiting examples listed in Table 1, a functional mutant, a variant or a derivative thereof. In another embodiment, said additional C-terminal domain of said engineered core TALE scaffold is an enhancer domain. In another embodiment, said enhancer domain is selected from the group consisting of hydrolase/transferase of Pseudomonas Aeuriginosa family, the polymerase domain from the Mycobacterium tuberculosis Ligase D family, the initiation factor elF2 from Pyrococcus family, the translation initiation factor Aif2 family as non-limiting examples. In another embodiment, said enhancer domain sequence is selected from the group consisting of protein domains of SEQ ID NO: 6 to SEQ ID NO: 9 as non-limiting examples listed in Table 1.

In another preferred embodiment, the catalytic domain that is capable of processing DNA nearby the single double-stranded DNA target sequence of interest, when fused to said engineered core TALE scaffold according to the present invention, is fused to the N-terminus part of said core TALE scaffold. In another preferred embodiment, said catalytic domain is fused to the C-terminus part of said core TALE scaffold. In another preferred embodiment two catalytic domains are fused to both N-terminus part of said core TALE scaffold and C-terminus part of said core TALE scaffold. In a more preferred embodiment, said catalytic domain has an enzymatic activity selected from the group consisting of nuclease activity, polymerase activity, kinase activity, phosphatase activity, methylase activity, topoisomerase activity, integrase activity, transposase activity or ligase activity. In another preferred embodiment, the catalytic domain fused to the core TALE scaffold of the present invention can be a transcription activator or repressor (i.e. a transcription regulator), or a protein that interacts with or modifies other proteins such as histones. Non-limiting examples of DNA processing activities of said compact TALEN of the present invention include, for example, creating or modifying epigenetic regulatory elements, making site-specific insertions, deletions, or repairs in DNA, controlling gene expression, and modifying chromatin structure.

In another more preferred embodiment, said catalytic domain has an endonuclease activity. In another more preferred embodiment, said catalytic domain of the compact TALEN according to the present invention has cleavage activity on said double-stranded DNA according to the method of the present invention. In another more preferred embodiment, said catalytic domain has a nickase activity on said double-stranded DNA according to the method of the present invention. In another more preferred embodiment, said catalytic domain is selected from the group consisting of proteins MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative thereof. In another preferred embodiment said catalytic domain of the compact TALEN according to the present invention is I-TevI (SEQ ID NO: 20), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain I-TevI (SEQ ID NO: 20), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the compact TALEN of the present invention. In another preferred embodiment, said compact TALEN according to the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 426-432.

In another preferred embodiment, said catalytic domain of the compact TALEN according to the present invention is ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain ColE7 (SEQ ID NO: 11), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 435-438.

In another preferred embodiment, said catalytic domain of the compact TALEN according to the present invention is NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain NucA (SEQ ID NO: 26), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, said compact TALEN according to the method of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 433-434.

In another preferred embodiment, said catalytic domain is I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof. In another preferred embodiment, catalytic domain I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof is fused to the N-terminal domain of said core TALE scaffold according to the method of the present invention. In another preferred embodiment, catalytic domain I-CreI (SEQ ID NO: 1), a functional mutant, a variant or a derivative thereof is fused to the C-terminal domain of said core TALE scaffold according to the present invention. In another preferred embodiment, said compact TALEN according to the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group of SEQ ID NO: 439-441 and SEQ ID NO: 444-446.

In another embodiment, said catalytic domain is a restriction enzyme such as MmeI, R-HinPII, R.MspI, R.MvaI, Nb.BsrDI, BsrDI A, Nt.BspD6I, ss.BspD6I, R.PleI, MlyI and AlwI as non-limiting examples listed in table 2. In another more preferred embodiment, said catalytic domain has an exonuclease activity. In another more preferred embodiment, any combinations of two catalytic domains selected from the group consisting of proteins MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative of these protein domains thereof, can be fused to both N-terminus part and C-terminus part of said core TALE scaffold, respectively. For example, I-HmuI catalytic domain can be fused to the N-terminus part of said core TALE scaffold and ColE7 catalytic domain can be fused to the C-terminus part of said core TALE scaffold. In another example, I-TevI catalytic domain can be fused to the N-terminus part of said core TALE scaffold and ColE7 catalytic domain can be fused to the C-terminus part of said core TALE scaffold.

Table 14 below gives non-limiting examples of combinations of catalytic domains that can be comprised in the compact TALEN monomer according to the present invention. Optionally, FokI (SEQ ID NO:368) can be used in combination with another catalytic domain according to the list of Table2.

TABLE 14 Examples of combinations of catalytic domains respectively fused to N and C-terminus part of compact TALEN core scaffolds according to the present invention leading to dual-cleavage TALENs. Catalytic domain Catalytic domain fused to N-terminus fused to C-terminus part of core TALE part of core TALE Dual-cleavage scaffold scaffold TALENS I-TevI I-TevI TevI-TevI ColE7 ColE7 ColE7-ColE7 NucA NucA NucA-NucA I-TevI ColE7 TevI-ColE7 I-TevI NucA TevI-NucA ColE7 I-TevI ColE7-TevI ColE7 NucA ColE7-NucA NucA I-TevI NucA-TevI NucA ColE7 NucA-ColE7

In a preferred embodiment according to the present invention, said unique compact TALEN monomer comprises a combination of two catalytic domains respectively fused to the N-terminus part and to the C-terminus part of said core TALE scaffold selected from the group consisting of:

-   -   (i) A Nuc A domain (SEQ ID NO: 26) in N-terminus and a Nuc A         domain (SEQ ID NO: 26) in C-terminus;     -   (ii) A ColE7 domain (SEQ ID NO: 11) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus;     -   (iii) A TevI domain (SEQ ID NO: 20) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus;     -   (iv) A TevI domain (SEQ ID NO: 20) in N-terminus and a NucA         domain (SEQ ID NO: 26) in C-terminus;     -   (v) A ColE7 domain (SEQ ID NO: 11) in N-terminus and a NucA         domain (SEQ ID NO: 26) in C-terminus;     -   (vi) A NucA domain (SEQ ID NO: 26) in N-terminus and a ColE7         domain (SEQ ID NO: 11) in C-terminus.

In another preferred embodiment, said compact TALEN according to the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 448 and 450.

In another preferred embodiment, said compact TALEN according to the present invention comprises a combination of two catalytic domains respectively fused to the C-terminus part and to the N-terminus part of said core TALE scaffold selected from the group consisting of:

-   -   (i) A TevI domain (SEQ ID NO: 20) in N-terminus and a FokI         domain (SEQ ID NO: 368) in C-terminus;     -   (ii) A TevI domain (SEQ ID NO: 20) in N-terminus and a TevI         domain (SEQ ID NO: 20) in C-terminus;     -   (iii) A scTrex2 domain (SEQ ID NO: 451) in N-terminus and a FokI         domain (SEQ ID NO: 368) in C-terminus.

In another preferred embodiment, said compact TALEN according to the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 447-450 and SEQ ID NO: 452.

In the scope of the present invention, it can be envisioned to insert said catalytic domain and/or said enhancer domain between two parts of the engineered core TALE scaffold according to the invention, each part comprising one set of RVDs. In this last case, the number of RVDs for each part of the engineered core TALE scaffold can be the same or not. In other words, it can be envisioned to split said core TALE scaffold of the present invention to insert one catalytic domain and/or one enhancer domain between the resulting two parts of said engineered core TALE scaffold. In another preferred embodiment, said compact TALEN according to the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 453-455.

In other words, the compact TALEN monomer of the present invention comprises a protein sequence having at least 80%, more preferably 90%, again more preferably 95% amino acid sequence identity with the protein sequences selected from the group consisting of SEQ ID NO: 420-450 and 452-455.

In another preferred embodiment according to the method of the present invention, the peptidic linker that can link said catalytic domain to the core TALE scaffold according to the method of the present invention can be selected from the group consisting of NFS1, NFS2, CFS1, RM2, BQY, QGPSG (SEQ ID NO: 469), LGPDGRKA (SEQ ID NO: 104), 1a8h_1, 1dnpA_1, 1d8cA_2, 1ckqA_3, 1sbp_1, 1ev7A_1, 1alo_3, 1amf_1, 1adjA_3, 1fcdC_1, 1a13_2, 10 1g3p_1, 1acc_3, 1ahjB_1, 1acc_1, 1af7_1, 1heiA_1, 1bia_2, 1igtB_1, 1nfkA_1, 1au7A_1, 1bpoB_1, 1b0 pA_2, 1c05A_2, 1gcb_1, 1bt3A_1, 1b3oB_2, 16vpA_6, 1dhx_1, 1b8aA_1and 1qu6A_1, as listed in Table 3 (SEQ ID NO: 67 to SEQ ID NO: 104 and SEQ ID NO: 372 to SEQ ID NO: 415). In a more preferred embodiment, the peptidic linker that can link said catalytic domain to the core TALE scaffold according to the method of the present invention can be selected from the group consisting of NFS1 (SEQ ID NO: 15 98), NFS2 (SEQ ID NO: 99) and CFS1 (SEQ ID NO: 100). In the scope of the present invention is also encompassed the case where a peptidic linker is not needed to fuse a catalytical domain to the TALE scaffold in order to obtain a cTALEN according to the present invention.

Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities and eventually type of linker(s)], a compact TALEN according to the present invention can comprise different levels of separate enzymatic activities able to differently process DNA, resulting in a global DNA processing efficiency for said compact TALEN, each one of said different enzymatic activities having their own DNA processing efficiency.

In another preferred embodiment, the compact TALEN according to the present invention further comprises:

-   -   (i) at least one enhancer domain;     -   (ii) Optionally one peptide linker to fuse said enhancer domain         to one part of said compact TALEN active entity;         thereby obtaining a compact TALEN entity with enhanced DNA         processing efficiency nearby a single double-stranded DNA target         sequence of interest, i.e. an enhanced compact TALEN.

In other words, said unique compact TALEN monomer further comprises:

-   -   (i) At least one enhancer domain;     -   (ii) Optionally one peptide linker to fuse said enhancer domain         to one part of said unique compact TALEN monomer active entity.

In another more preferred embodiment, said enhancer domain is fused to N-terminus of the core TALE scaffold part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused to C-terminus of the core TALE scaffold part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused to the catalytic domain part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused between the N-terminus part of the core TALE scaffold and the catalytic part of said compact TALEN entity. In another more preferred embodiment, said enhancer domain is fused between the C-terminus part of the core TALE scaffold and the catalytic part of said compact TALEN entity. In the scope of the present invention, it can be envisioned to insert said catalytic domain and/or enhancer domain between two parts of the engineered core TALE scaffold according to the invention, each part comprising one set of RVDs. In this last case, the number of RVDs for each engineered core TALE scaffold can be the same or not. In other words, it can be envisioned to split said core TALE scaffold of the present invention to insert one catalytic domain and/or one enhancer domain between the resulting two parts of said engineered core TALE scaffold.

In another preferred embodiment, said enhancer domain is catalytically active or not, providing functional and/or structural support to said compact TALEN entity. In a more preferred embodiment, said enhancer domain consists of a protein domain selected from the group consisting of MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MIyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative of these protein domains thereof. In another more preferred embodiment, said enhancer domain consists of a catalytically active derivative of the protein domains listed above and in Table 2, providing functional and/or structural support to said compact TALEN entity. In another preferred embodiment, said enhancer domain consists of a catalytically inactive derivative of the protein domains listed above and in Table 2, providing structural support to said compact TALEN entity. In another preferred embodiment, said enhancer domain is selected from the group consisting of I-TevI (SEQ ID NO: 20), ColE7 (SEQ ID NO: 11) and NucA (SEQ ID NO: 26).

In a more preferred embodiment, said enhanced compact TALEN according to the present invention can comprise a second enhancer domain. In this embodiment, said second enhancer domain can have the same characteristics than the first enhancer domain. In a more preferred embodiment, said second enhancer domain provides structural support to enhanced compact TALEN entity. In another more preferred embodiment, said second enhancer domain provides functional support to enhanced compact TALEN entity. In a more preferred embodiment, said second enhancer domain provides structural and functional supports to enhanced compact TALEN entity. In a more preferred embodiment, said enhanced compact TALEN entity comprises one catalytic domain and one enhancer domain. In another more preferred embodiment said enhanced compact TALEN entity comprises one catalytic domain and two enhancer domains. In another more preferred embodiment said enhanced compact TALEN entity comprises two catalytic domains and one enhancer domains. In another more preferred embodiment said enhanced compact TALEN entity comprises two catalytic domains and two enhancer domains.

In a more preferred embodiment, said second enhancer domain consists of a protein domain derived from a protein selected from the group consisting of MmeI, Colicin-E7 (CEA7_ECOLX), Colicin-E9, APFL, EndA, Endo I (END1_ECOLI), Human Endo G (NUCG_HUMAN), Bovine Endo G (NUCG_BOVIN), R.HinP1I, I-BasI, I-BmoI, I-HmuI, I-TevI, I-TevII, I-TevIII, I-TwoI, R.MspI, R.MvaI, NucA, NucM, Vvn, Vvn_CLS, Staphylococcal nuclease (NUC_STAAU), Staphylococcal nuclease (NUC_STAHY), Micrococcal nuclease (NUC_SHIFL), Endonuclease yncB, Endodeoxyribonuclease I (ENRN_BPT7), Metnase, Nb.BsrDI, BsrDI A, Nt.BspD6I (R.BspD6I large subunit), ss.BspD6I (R.BspD6I small subunit), R.PleI, MlyI, AlwI, Mva1269I, BsrI, BsmI, Nb.BtsCI, Nt.BtsCI, R1.BtsI, R2.BtsI, BbvCI subunit 1, BbvCI subunit 2, Bpu10I alpha subunit, Bpu10I beta subunit, BmrI, BfiI, I-CreI, hExol (EXO1_HUMAN), Yeast Exol (EXO1_YEAST), E. coli Exol, Human TREX2, Mouse TREX1, Human TREX1, Bovine TREX1, Rat TREX1, Human DNA2, Yeast DNA2 (DNA2_YEAST) and VP16, as listed in Table 2 (SEQ ID NO: 10 to SEQ ID NO: 66 and SEQ ID NO: 1, 366 & 367), a functional mutant, a variant or a derivative of these protein domains thereof. In another more preferred embodiment, said second enhancer domain consists of a catalytically active derivative of the protein domains listed above and in Table 2, providing functional and/or structural support to said enhanced compact TALEN entity. In another preferred embodiment, said second enhancer domain consists of a catalytically inactive derivative of the protein domains listed above and in Table 2, providing structural support to said enhanced compact TALEN entity.

In another more preferred embodiment, any combinations of catalytic and/or enhancer domains listed above, as non-limiting examples, can be envisioned to be fused to said core TALE scaffold providing structural and/or functional support to said compact TALEN entity. More preferably, combinations of catalytic domains listed in Table 14. Again more preferably, combinations of catalytic domains selected from the group of TevI (SEQ ID NO: 20), ColE7 (SEQ ID NO: 11) and NucA (SEQ ID NO: 26) can be envisioned. Optionally, FokI (SEQ ID NO: 368) can be used in combination with another catalytic domain according to the list of Tablet. Such combinations of catalytic and/or enhancer domains can be envisioned regarding the envisioned applications for using the method of the present invention. Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities, type of linker(s) and type of enhancer(s) domains], an enhanced compact TALEN according to the present invention can present different levels of separate enzymatic activities able to differently process DNA, resulting in a global DNA processing efficiency for said enhanced compact TALEN, each one of said different enzymatic activities having their own DNA processing efficiency.

In this preferred embodiment, the DNA processing efficiency of the compact TALEN entity according to the present invention can be enhanced by the engineering of at least one enhancer domain and one peptidic linker thereby obtaining a compact TALEN entity with enhanced DNA processing activity nearby a single double-stranded DNA target sequence of interest, i.e. a enhanced compact TALEN according to the present invention.

Depending from its structural composition, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention, can have a dominant enzymatic activity selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In a more preferred embodiment, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention is a combination of different enzymatic activities selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In a more preferred embodiment, the global DNA processing efficiency that is enhanced in said enhanced compact TALEN according to the present invention is one of its different enzymatic activities selected from the group consisting of a nuclease activity, a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. In this case, the global DNA processing efficiency is equivalent to one DNA processing activity amongst the enzymatic activities mentioned above. In another more preferred embodiment, said DNA processing activity of the compact TALEN entity which is enhanced by the enhancer is a cleavase activity or a nickase activity or a combination of both a cleavase activity and a nickase activity.

Enhancement of DNA processing efficiency of a compact TALEN entity according to the present invention can be a consequence of a structural support by said at least one enhancer domain. In a preferred embodiment, said structural support enhances the binding of a compact TALEN entity according to the invention for said DNA target sequence compared to the binding of a starting compact TALEN entity for the same DNA target sequence, thereby indirectly assisting the catalytic domain(s) to obtain a compact TALEN entity with enhanced DNA processing activity. In another preferred embodiment, said structural support enhances the existing catalytical activity of a compact TALEN entity for a DNA target sequence compared to the binding of a starting compact TALEN entity for the same DNA target sequence to obtain a compact TALEN entity with enhanced DNA processing activity.

In another preferred embodiment, said enhancer according to the present invention both enhances the binding of the compact TALEN entity for said DNA target sequence and the catalytic activity of the catalytic domain(s) to obtain a compact TALEN entity with enhanced DNA processing activity. All these non-limiting examples lead to a compact TALEN entity with enhanced DNA processing efficiency for a DNA target sequence at a genomic locus of interest, i.e. an enhanced compact TALEN according to the present invention.

Enhancement of DNA processing efficiency of a compact TALEN entity according to the present invention, compared to a starting compact TALEN entity, can also be a consequence of a fuctional support by said at least one enhancer domain. In a preferred embodiment, said functional support can be the consequence of the hydrolysis of additional phosphodiester bonds. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a nuclease. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from an endonuclease. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a cleavase. In another more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from a nickase. In a more preferred embodiment, said functional support can be the hydrolysis of additional phosphodiester bonds by a protein domain derived from an exonuclease.

In genome engineering experiments, the efficiency of rare-cutting endonuclease, e.g. their ability to induce a desired event (Homologous gene targeting, targeted mutagenesis, sequence removal or excision) at a locus, depends on several parameters, including the specific activity of the nuclease, probably the accessibility of the target, and the efficacy and outcome of the repair pathway(s) resulting in the desired event (homologous repair for gene targeting, NHEJ pathways for targeted mutagenesis).

Cleavage by peptidic rare cutting endonucleases usually generates cohesive ends, with 3′ overhangs for LAGLIDADG meganucleases (Chevalier and Stoddard 2001) and 5′ overhangs for Zinc Finger Nucleases (Smith, Bibikova et al. 2000). These ends, which result from hydrolysis of phosphodiester bonds, can be re-ligated in vivo by NHEJ in a seamless way (i.e. a scarless re-ligation). The restoration of a cleavable target sequence allows for a new cleavage event by the same endonuclease, and thus, a series of futile cycles of cleavage and re-ligation events can take place. Indirect evidences have shown that even in the yeast Saccharomyces cerevisiae, such cycles could take place upon continuous cleavage by the HO endonuclease (Lee, Paques et al. 1999). In mammalian cells, several experiment have shown that perfect re-ligation of compatible cohesive ends resulting from two independent but close I-SceI-induced DSBs is an efficient process (Guirouilh-Barbat, Huck et al. 2004; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Cheng et al. 2008; Bennardo, Gunn et al. 2009). Absence of the Ku DNA repair protein does not significantly affect the overall frequency of NHEJ events rejoining the ends from the two DSBs; however it very strongly enhances the contribution of imprecise NHEJ to the repair process in CHO immortalized cells and mouse ES cells (Guirouilh-Barbat, Huck et al. 2004; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Cheng et al. 2008). Furthermore, the absence of Ku stimulates I-SceI-induced events such as imprecise NHEJ (Bennardo, Cheng et al. 2008), single-strand annealing (Bennardo, Cheng et al. 2008) and gene conversion (Pierce, Hu et al. 2001; Bennardo, Cheng et al. 2008) in mouse ES cells. Similar observations shave been made with cells deficient for the XRCC4 repair protein (Pierce, Hu et al. 2001; Guirouilh-Barbat, Rass et al. 2007; Bennardo, Gunn et al. 2009) (although XRCC4 deficiency affects the overal level of NHEJ in CHO cells (Guirouilh-Barbat, Rass et al. 2007)) or for DNA-PK (Pierce, Hu et al. 2001). In contrast, knock-down of CtIP has been shown to suppresses “alt-NHEJ” (a Ku- and XRCC4-independent form of NHEJ more prone to result in imprecise NHEJ), single-strand annealing and gene conversion, while not affecting the overall level of rejoining of two compatible ends generated by I-SceI (Bennardo, Cheng et al. 2008). Thus, competition between different DSB repair pathways can affect the spectrum or repair events resulting from a nuclease-induced DSB.

In addition, DSB resection is important for certain DSB pathways. Extensive DSB resection, resulting in the generation of large single stranded regions (a few hundred nucleotides at least), has been shown in yeast to initiate single strand annealing (Sugawara and Haber 1992) and strand invasion, the ATP-dependant step that initiates many homologous recombination events of DNA duplex invasion by an homologous strand that (White and Haber 1990; Sun, Treco et al. 1991) (for a review of mechanisms, see (Paques and Haber 1999)). In eukaryotic cells DSB resection depends on several proteins including BLM/Sgs1 and DNA2, EXOI, and the MRN complex (Mre11, Rad50, Nbs1/Xrs2) and is thought to result from different pathways. MRN is involved in a small scale resection process, while two redundant pathways depending on BLM and DNA2 on one hand, and on EXOI on another hand, would be involved in extensive resection (Mimitou and Symington 2008; Nimonkar, Genschel et al. 2011). In addition, processing ends involving a damaged nucleotide (resulting from chemical cleavage or from a bulk adduct), requires the CtIP/Sae2 protein together with RMN (Sartori, Lukas et al. 2007; Buis, Wu et al. 2008; Hartsuiker, Mizuno et al. 2009). Over-expression of the Trex2 exonuclease was shown to strongly stimulate imperfect NHEJ associated with loss of only a few base pairs (Bennardo, Gunn et al. 2009), while it inhibited various kinds of DNA repair events between distant sequences (such as Single-strand annealing, NHEJ between ends from different breaks, or NHEJ repair of a single DSB involving remote micro-homologies). In the same study, it was suggested that Trex2 did resect the 3′ overhangs let by I-SceI in a non processive way. Thus, the type of stimulated pathway could in turn depend on the type of resection (length of resection, single strand vs. double strand, resection of 5′ strand vs. 3′ strand).

Thus, the efficiency of a compact TALEN, e.g. it ability to produce a desired event such as targeted mutagenesis or homologous gene targeting (see definition for full definition of “efficiency of compact TALEN”), can be enhanced by an enhancement or modification of its global DNA processing efficiency (see definition for full definition of “global DNA processing efficiency”), e.g. the global resultant or the overall result of different separate enzymatic activities that said compact TALEN.

In a preferred embodiment, enhancement of global DNA processing efficiency of a compact TALEN entity according to the present invention, compared to a starting compact TALEN entity, can be the hydrolysis of additional phosphodiester bonds at the cleavage site.

Said hydrolysis of additional phosphodiester bonds at the cleavage site by said at least one enhancer according to the invention can lead to different types of DSB resection affecting at said DSB cleavage site, one single DNA strand or both DNA strands, affecting either 5′ overhangs ends, either 3′ overhangs ends, or both ends and depending on the length of said resection. Thus, adding new nickase or cleavase activities to the existing cleavase activity of a compact TALEN entity can enhance the efficiency of the resulting enhanced compact TALEN according to the invention, at a genomic locus of interest (FIG. 8B-8E). As a non-limiting example, addition of two nickase activities on opposite strands (FIG. 8D) or of a new cleavase activity generating a second DSB (FIG. 8E) can result in a double-strand gap. As a consequence, perfect religation is not possible anymore, and one or several alternative repair outcomes such as imprecise NHEJ, Homologous Recombination or SSA for instance, can be stimulated. As another non-limiting example, the addition of a single nickase activity can result in a single strand gap, and suppress the cohesivity of the ends, which can also enhances the efficiency of the resulting enhanced compact TALEN at a genomic locus of interest, according to the invention, via stimulation of one or several alternative repair outcomes mentioned above.

In this aspect of the present invention, enhancement of DNA processing efficiency of a compact TALEN refers to the increase in the detected level of said DNA processing efficiency, against a target DNA sequence, of a compact TALEN in comparison to the activity of a first compact TALEN against the same target DNA sequence. Said first compact TALEN can be a starting compact TALEN, or a compact TALEN that has already been engineered or an enhanced compact TALEN according to the present invention. Several rounds of enhancement can be envisioned from a starting compact TALEN or from a starting enhanced compact TALEN.

In this aspect of the present invention, enhancement of the DNA processing efficiency of the compact TALEN entity (or enhanced compact TALEN) refers to the increase in the detected level of said DNA processing efficiency against a target DNA sequence of interest or nearby said DNA sequence of interest in comparison to the efficiency of a first compact TALEN or starting compact TALEN against or nearby the same target DNA sequence. In this case, the starting compact TALEN is taken as the reference scaffold to measure the DNA processing efficiency. Said enhanced compact TALEN is an engineered compact TALEN comprising an enhancer domain according to this aspect of the invention. Said enhanced compact TALEN can also be taken as a reference scaffold for further enhancement in said DNA processing efficiency. As a non-limiting example, said DNA processing efficiency can result from a cleavage-induced recombination generated by said enhanced compact TALEN. In this case, said level of cleavage-induced recombination can be determined, for instance, by a cell-based recombination assay as described in the International PCT Application WO 2004/067736. Importantly, enhancement of efficacy in cells (enhanced generation of targeted mutagenesis or targeted recombination) can be, but is not necessarily associated with an enhancement of the cleavage activity that could be detected in certain in vitro assays. For example, additional phosphodiesterase activities as described in FIG. 8 could barely affect the cleavage profile, as detected by in vitro cleavage and separation of the cleavage products on an electrophoresis gel. However, as explained above, and in the legend of FIG. 8, the DSB ends generated in this way could be more prone to induce detectable genomic rearrangements such as targeted mutagenesis (by imprecise NHEJ) or homologous recombination. Said enhancement in cleavage-induced recombination of said enhanced compact TALEN is at least a 5% enhancement compared to the starting scaffold or starting compact TALEN, more preferably at least a 10% enhancement, again more preferably at least a 15% enhancement, again more preferably at least a 20% enhancement, again more preferably at least a 25% enhancement, again more preferably a 50% enhancement, again more preferably a enhancement greater than 50%, resulting in an enhancement of DNA processing efficiency of said enhanced compact TALEN of at least 5% compared to the starting scaffold or starting compact TALEN, more preferably at least a 10% enhancement, again more preferably at least a 15% enhancement, again more preferably at least a 20% enhancement, again more preferably at least a 25% enhancement, again more preferably a 50% enhancement, again more preferably a enhancement greater than 50%.

In another preferred embodiment according to the method of the present invention, the peptidic linker that can link said enhancer domain to one part of said compact TALEN entity according to the method of the present invention can be selected from the group consisting of NFS1, NFS2, CFS1, RM2, BQY, QGPSG (SEQ ID NO: 469), LGPDGRKA (SEQ ID NO: 104), 1a8h_1, 1dnpA_1, 1d8cA_2, 1ckqA_3, 1sbp_1, 1ev7A_1, 1alo_3, 1amf_1, 1adjA_3, 1fcdC_1, 1a13_2, 1g3p_1, 1acc_3, 1ahjB_1, 1acc_1, 1af7_1, 1heiA_1, 1bia_2, 1igtB_1, 1nfkA_1, 1au7A_1, 1bpoB_1, 1b0 pA_2, 1c05A_2, 1gcb_1, 1bt3A_1, 1b3oB_2, 16vpA_6, 1dhx_1, 1b8aA_1 and 1qu6A_1 as listed in table 3 (SEQ ID NO: 67 to SEQ ID NO: 104 and SEQ ID NO: 372 to SEQ ID NO: 415). In a more preferred embodiment, the peptidic linker that can said enhancer domain to one part of said compact TALEN entity according to the method of the present invention can be selected from the group consisting of NFS1 (SEQ ID NO: 98), NFS2 (SEQ ID NO: 99) and CFS1 (SEQ ID NO: 100). In the scope of the present invention is also encompassed the case where a peptidic linker is not needed to fuse one enhancer domain to one part of said compact TALEN entity in order to obtain a enhanced compact TALEN according to the present invention.

Depending from its structural composition [type of core TALE scaffold, type of catalytic domain(s) with associated enzymatic activities, type of enhancers and eventually type of linker(s)], a compact TALEN or an enhanced compact TALEN according to the present invention can comprise different levels of separate enzymatic activities able to differently process DNA as mentioned above. By adding new enzymatic activities to said compact TALEN or enhanced compact TALEN or enhancing the DNA processing efficiency of one or several of its constitutive enzymatic activities, one can enhance the global DNA processing efficiency of one compact TALEN or enhanced compact TALEN in comparison to a starting compact TALEN or enhanced compact TALEN.

According to the present invention, compact TALENs are designed to alleviate the need for multiple independent protein moieties when targeting a DNA processing event. Importantly, the requisite “spacer” region and dual target sites essential for the function of current TALENs are unnecessary, as compact TALENs according to the invention comprises a core TALE scaffold containing only one DNA binding domain to target a specific single double-stranded DNA target sequence of interest and process DNA nearby said single double-stranded DNA target sequence of interest. As each end of the core TALE scaffold is amenable to fusion, the order (N- v.s C-terminal) of addition of the catalytic and enhancement domains can vary with the application. In addition, since the catalytic domain does not require specific DNA contacts, there are no restrictions on regions surrounding the core TALE scaffold, as non-limiting examples depicted in FIG. 5: (A) N-terminal fusion construct to promote Homologous recombination induced by a cleavase domain or by a nickase domain. (B) C-terminal fusion construct with properties as in (A). (C) The attachment of two catalytic domains to both ends of the core TALE scaffold allows for dual cleavage with enhancement in NHEJ. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application.

According to the present invention, compact TALENs can be enhanced through the addition of a domain to promote existing or alternate activities as non-limiting examples depicted in FIG. 6: (A) A standard compact TALEN with an enhancer domain fused to the C-terminus of its core TALE scaffold part. (B) The enhancer domain is fused to the compact TALEN via the N-terminus of its catalytic domain part. Such a configuration can be used to assist and/or anchor the catalytic domain part near the DNA to increase DNA processing activity. (C) The enhancer domain is sandwiched between the catalytic domain part and the core TALE scaffold part. The enhancer domain can promote communication between the flanking domains (i.e. to assist in catalysis and/or DNA binding) or can be used to overcome the requisite T nucleotide at position −1 of all TALE-based targets. (D) The enhancer domain is used to functionally replace the engineered core TALE scaffold N-terminal region. (E) The enhancer domain is used to functionally replace the engineered core TALE scaffold C-terminal region. Fusion junctions (N-vs. C-terminal) and linker designs can vary with the application.

According to the present invention, the nature of the catalytic domain(s) comprised in the compact TALEN and the enhanced compact TALEN is application dependent. As a non-limiting example, a nickase domain should allow for a higher HR/NHEJ ratio than a cleavase domain, thereby being more agreeable for therapeutic applications (McConnell Smith, Takeuchi et al. 2009; Metzger, McConnell-Smith et al. 2011). For example, the coupling of a cleavase domain on one side with a nickase domain on the other could result in excision of a single-strand of DNA spanning the binding region of a compact TALEN. The targeted generation of extended single-strand overhangs could be applied in applications that target DNA repair mechanisms. For targeted gene inactivation, the use of two cleavase domains is then preferred. In another preferred embodiment, the use of two nickase domains can be favored. Furthermore, the invention relates to a method for generating several distinct types of compact TALENs that can be applied to applications ranging from targeted DNA cleavage to targeted gene regulation.

The present invention also relates to methods for use of said compact TALENs according to the invention for various applications ranging from targeted DNA cleavage to targeted gene regulation. In a preferred embodiment, the present invention relates to a method for increasing targeted HR (and NHEJ) when Double-Strand break activity is promoted in a compact TALEN targeting a DNA target sequence according to the invention. In another more preferred embodiment, the addition of at least two catalytically active cleavase enhancer domains according to the invention allows to increase Double-strand break-induced mutagenesis by leading to a loss of genetic information and preventing any scarless re-ligation of targeted genomic locus of interest by NHEJ.

In another preferred embodiment, the present invention relates to a method for increasing targeted HR with less NHEJ (i.e. in a more conservative fashion) when Single-Strand Break activity is promoted in a compact TALEN targeting a DNA target sequence according to the invention.

In another preferred embodiment, the present invention relates to a method for increasing excision of a single-strand of DNA spanning the binding region of a compact TALEN when both one cleavase enhancer domain and one nickase enhancer domain, respectively, are fused to both N-terminus and C-terminus of a core TALE scaffold according to the invention.

In another preferred embodiment, the present invention relates to a method for treatment of a genetic disease caused by a mutation in a specific single double-stranded DNA target sequence in a gene, comprising administering to a subject in need thereof an effective amount of a variant of a compact TALEN according to the present invention.

In another preferred embodiment, the present invention relates to a method for inserting a transgene into a specific single double-stranded DNA target sequence of a genomic locus of a cell, tissue or non-human animal, or a plant wherein at least one compact TALEN of the present invention is transitory or not introduced into said cell, tissue, non-human animal or plant.

In another embodiment, the present invention relates to a method to modulate the activity of a compact TALEN when expressed in a cell wherein said method comprises the step of introducing in said cell an auxiliary domain modulating the activity of said compact TALEN. In a preferred embodiment, the present invention relates to a method which allows to have a temporal control of activity of a compact TALEN when expressed in a cell by introducing in said cell an auxiliary domain modulating the activity of said compact TALEN once said compact TALEN achieved its activity (DNA cleavage, DNA nicking or other DNA processing activities). In a preferred embodiment, the present invention relates to a method to inhibit the activity of a compact TALEN when expressed in a cell wherein said method comprises the step of introducing in said cell an auxiliary domain inhibiting the activity of said compact TALEN. In a more preferred embodiment, the catalytic domain of said compact TALEN is NucA (SEQ ID NO: 26) and said auxiliary domain is NuiA (SEQ ID NO: 229), a functional mutant, a variant or a derivative thereof. In another more preferred embodiment, the catalytic domain of said compact TALEN is ColE7 (SEQ ID NO: 11) and said auxiliary domain is Im7 (SEQ ID NO: 230), a functional mutant, a variant or a derivative thereof.

Is also encompassed in the scope of the present invention a recombinant polynucleotide encoding a compact TALEN, a dual compact TALEN, or an enhanced compact TALEN according to the present invention. Is also encompassed in the scope of the present invention, a vector comprising a recombinant polynucleotide encoding for a compact TALEN or an enhanced compact TALEN according to the present invention.

Is also encompassed in the scope of the present invention, a host cell which comprises a vector and/or a recombinant polynucleotide encoding for a compact TALEN or an enhanced compact TALEN according to the present invention.

Is also encompassed in the scope of the present invention, a non-human transgenic animal comprising a vector and/or a recombinant polynucleotide encoding for a compact TALEN or an enhanced compact TALEN according to the present invention.

Is also encompassed in the scope of the present invention, a transgenic plant comprising a vector and/or a recombinant polynucleotide encoding for a compact TALEN or an enhanced compact TALEN according to the present invention.

The present invention also relates to kits used to implement the method according to the present invention. More preferably, is encompassed in the scope of the present invention, a kit comprising a compact TALEN or an enhanced compact TALEN according to the present invention and instructions for use said kit in enhancing DNA processing efficiency of a single double-stranded DNA target sequence of interest.

For purposes of therapy, the compact TALENs of the present invention and a pharmaceutically acceptable excipient are administered in a therapeutically effective amount. Such a combination is said to be administered in a “therapeutically effective amount” if the amount administered is physiologically significant. An agent is physiologically significant if its presence results in a detectable change in the physiology of the recipient. In the present context, an agent is physiologically significant if its presence results in a decrease in the severity of one or more symptoms of the targeted disease and in a genome correction of the lesion or abnormality. Vectors comprising targeting DNA and/or nucleic acid encoding a compact TALEN can be introduced into a cell by a variety of methods (e.g., injection, direct uptake, projectile bombardment, liposomes, electroporation). Compact TALENs can be stably or transiently expressed into cells using expression vectors. Techniques of expression in eukaryotic cells are well known to those in the art. (See Current Protocols in Human Genetics: Chapter 12 “Vectors For Gene Therapy” & Chapter 13 “Delivery Systems for Gene Therapy”).

In one further aspect of the present invention, the compact TALEN of the present invention is substantially non-immunogenic, i.e., engender little or no adverse immunological response. A variety of methods for ameliorating or eliminating deleterious immunological reactions of this sort can be used in accordance with the invention. In a preferred embodiment, the compact TALEN is substantially free of N-formyl methionine. Another way to avoid unwanted immunological reactions is to conjugate compact TALEN to polyethylene glycol (“PEG”) or polypropylene glycol (“PPG”) (preferably of 500 to 20,000 daltons average molecular weight (MW)). Conjugation with PEG or PPG, as described by Davis et al. (U.S. Pat. No. 4,179,337) for example, can provide non-immunogenic, physiologically active, water soluble compact TALEN conjugates with anti-viral activity. Similar methods also using a polyethylene—polypropylene glycol copolymer are described in Saifer et al. (U.S. Pat. No. 5,006,333).

In another aspect of the present invention is a composition comprising a compact TALEN or an enhanced compact TALEN according to the present invention and a carrier. More preferably, is a pharmaceutical composition comprising a compact TALEN or an enhanced compact TALEN according to the present invention and a pharmaceutically active carrier known in the state of the art.

In the scope of the present invention and for all the applications mentioned above, it can be envisioned to use more than one compact TALEN (i.e. one compact TALEN active entity) or more than one enhanced compact TALENs (i.e. one enhanced compact TALEN active entity) for DNA processing according to the invention. In a preferred embodiment, two different compact TALENs or two enhanced compact TALENs can be used. In this embodiment, as non-limiting examples, said two different compact TALENs can comprise the same core TALE scaffold or not; said two different compact TALENs can comprise the same set of Repeat Variable Dipeptides or not; said two different compact TALENs can comprise the same catalytic domain or not. When two identical compact TALENs active entities are used for DNA processing according to the invention, they can be considered as a homodimeric pair of compact TALENs active entities. When two non identical compact TALENs active entities are used for DNA processing according to the invention, they can be considered as a heterodimeric pair of compact TALENs active entities. As non-limiting example, when two compact TALEN according to the present invention are used, one of the compact TALEN can modulate the activity of the other one, leading for instance to an enhanced DNA processing event compared to the same DNA processing event achieved by only one compact TALEN; in this non-limiting example, a Trans-TALEN modulates and enhances the catalytic activity of an initial compact TALEN.

In another preferred embodiment, three compact TALENs or three enhanced compact TALENs can be used. In another preferred embodiment, more than three compact TALENs or three enhanced compact TALENs can be used for DNA processing according to the invention. In another preferred embodiment, a combination of compact TALENs and enhanced compact TALENs can be used for DNA processing according to the invention. As a non-limiting example, one compact TALEN and one enhanced compact TALEN can be used. As another non-limiting example, one compact TALEN and one dual-cleavage compact TALEN can be used. In another preferred embodiment, a combination of compact TALENs, enhanced compact TALENs and dual-cleavage compact TALENs can be used, said compact TALENs comprising the same catalytic domain or not, the same core TALE scaffold or not. When several compact TALENs have to be used, DNA target sequence for each compact TALENs of the combination to be used can be located on a same endogenous genomic DNA locus of interest or not. Said DNA target sequences can be located at an approximative distance of 1000 base pairs (bps). More preferably, said DNA target sequences can be located at an approximative distance of 500 bps or 200 bps, or 100 bps, or 50 bps, or bps, 19 bps, 18 bps, 17 bps, 16 bps, 15 bps, 14 bps, 13 bps, 12 bps, 11 bps, 10 bps, 9 bps, 8 bps, 7 bps, 6 bps, 5 bps, 4 bps, 3 bps, 2 bps, 1 bp. Said DNA target sequences located at distances mentioned above are “nearby” DNA sequences in reference to the target DNA sequence for DNA processing according to the present invention.

In another preferred embodiment, two compact TALENs active entities can be used as a way of achieving two different DNA processing activities nearby a DNA target sequence according to the invention. As a non-limiting example, two compact TALENs targeting said DNA sequence or DNA sequences nearby said targeted DNA sequence and comprising each one a nickase-derived catalytic domain can be used; in this case, this use of two compact TALENs active entities can represent an alternative way of achieving a Double Strand Break nearby a said DNA target sequence, compared to the use of one compact TALEN targeting said DNA sequence and comprising a cleavase-derived catalytic domain, or not. As another non-limiting example, one compact TALEN comprising a cleavase-derived domain and one compact TALEN comprising an exonuclease-derived domain can be used to make a Double Strand Break and create a gap, respectively, to achieve an imprecise NHEJ event at the genomic locus of interest comprising said DNA target sequence. In this case, even if each compact TALEN forming this heterodimeric pair of compact TALENs is active by itself, each of these active entities is dependent of the other one to achieve the wanted resulting DNA processing activity. Indeed, in this particular case, the wanted resulting activity is a gap created by the exonuclease activity, said exonuclease activity being possible only from the Double Strand Break achieved by the cleavase domain of the other compact TALENs. In the scope of the present invention, is also envisioned the case where two identical compact TALEN active entities (a homodimeric pair of compact TALENs) are dependent each other to achieve a wanted resulting DNA processing activity.

DEFINITIONS

-   -   Amino acid residues in a polypeptide sequence are designated         herein according to the one-letter code, in which, for example,         Q means Gln or Glutamine residue, R means Arg or Arginine         residue and D means Asp or Aspartic acid residue.     -   Amino acid substitution means the replacement of one amino acid         residue with another, for instance the replacement of an         Arginine residue with a Glutamine residue in a peptide sequence         is an amino acid substitution.     -   Enhanced/increased/improved DNA processing activity, refers to         an increase in the detected level of a given compact TALEN or         enhanced compact TALEN associated DNA processing activity         against a target DNA sequence or DNA target sequence by a second         compact TALEN or enhanced compact TALEN in comparison to the         activity of a first compact TALEN or enhanced compact TALEN         against the target DNA sequence. The second compact TALEN or         enhanced compact TALEN can be a variant of the first one and can         comprise one or more substituted amino acid residues in         comparison to the first compact TALEN or enhanced compact TALEN.         The second compact TALEN or enhanced compact TALEN can be a         variant of the first one and can comprise one or more catalytic         and/or enhancer domains in comparison to said first compact         TALEN or enhanced compact TALEN. This definition more broadly         applies for other endonucleases and rare-cutting endonucleases.     -   DNA processing activity refers to a particular/given enzymatic         activity of said compact TALEN or enhanced compact TALEN or more         broadly to qualify the enzymatic activity of a rare-cutting         endonuclease. Said DNA processing activity can refer to a         cleavage activity, either a cleavase activity either a nickase         activity, more broadly a nuclease activity but also a polymerase         activity, a kinase activity, a phosphatase activity, a methylase         activity, a topoisomerase activity, an integrase activity, a         transposase activity or a ligase activity as non-limiting         examples. In the scope of this definition, said given DNA         processing activity of a particular enzymatic activity can also         be described as DNA processing efficiency of said particular         enzymatic activity. Methods for enhancing compact TALEN or         enhanced compact TALEN DNA processing activity according to this         definition are encompassed in the present invention.     -   Global DNA processing efficiency describes, for a compact TALEN         or an enhanced compact TALEN according to the present invention,         the global resultant or the overall effect of different separate         enzymatic activities that said compact TALEN or enhanced compact         TALEN can comprise. According to these different separate         enzymatic activities, a compact TALEN or an enhanced compact         TALEN presents a global capacity to process DNA nearby a target         sequence in a genomic locus of interest, i.e. a global DNA         processing efficiency. Said global DNA processing efficiency can         qualify or rank a second given compact TALEN or enhanced compact         TALEN in comparison to a first given compact TALEN or enhanced         compact TALEN. Depending on said compact TALENs or enhanced         compact TALENs structural composition [type of core TALE         scaffold, type of catalytic domain(s) with associated enzymatic         activities, eventually type of linker(s) and type of enhancer(s)         domains], said global DNA processing efficiency can refer to         only one enzymatic activity, two enzymatic activities, three         enzymatic activities, four enzymatic activities or more than         four enzymatic activities. Said global DNA processing efficiency         can refer to the sum of individual enzymatic activities. Said         global DNA processing efficiency can refer to the synergy or         combined effect of different enzymatic activities comprised in a         given compact TALEN or enhanced compact TALEN. An enhancement of         the DNA processing efficiency of a compact TALEN according to         the present invention can reflect a synergy, an enhanced         combined effect, resulting in an enhanced compact TALEN         characterized by a global DNA processing efficiency that is         greater than the sum of respective DNA processing efficiencies         of separate starting compact TALEN or than the sum of respective         DNA processing efficiencies of separate enzymatic activities         comprised in a same starting compact TALEN.     -   Efficiency of a rare-cutting endonuclease according to the         present invention is the property for said rare-cutting         endonuclease of producing a desired event. This desired event         can be for example Homologous gene targeting, targeted         mutagenesis, or sequence removal or excision. The efficiency of         the desired event depends on several parameters, including the         specific activity of the nuclease and the repair pathway(s)         resulting in the desired event (efficacy of homologous repair         for gene targeting, efficacy and outcome of NHEJ pathways for         targeted mutagenesis). Efficiency of a rare cutting endonuclease         for a locus is intended to mean its ability to produce a desired         event at this locus. Efficiency of a rare cutting endonuclease         for a target is intended to mean its ability to produce a         desired event as a consequence of cleavage of this target.     -   Nucleotides are designated as follows: one-letter code is used         for designating the base of a nucleoside: a is adenine, t is         thymine, c is cytosine, and g is guanine. For the degenerated         nucleotides, r represents g or a (purine nucleotides), k         represents g or t, s represents g or c, w represents a or t, m         represents a or c, y represents t or c (pyrimidine nucleotides),         d represents g, a or t, v represents g, a or c, b represents g,         t or c, h represents a, t or c, and n represents g, a, t or c.     -   by “meganuclease”, is intended a rare-cutting endonuclease         subtype having a double-stranded DNA target sequence greater         than 12 bp. Said meganuclease is either a dimeric enzyme,         wherein each domain is on a monomer or a monomeric enzyme         comprising the two domains on a single polypeptide.     -   by “meganuclease domain” is intended the region which interacts         with one half of the DNA target of a meganuclease and is able to         associate with the other domain of the same meganuclease which         interacts with the other half of the DNA target to form a         functional meganuclease able to cleave said DNA target.     -   by “endonuclease variant”, “rare-cutting endonuclease variant”,         “chimeric rare-cutting endonuclease variant” or “meganuclease         variant” or “compact TALEN variant”, or “enhanced compact TALEN         variant” or “dual cleavage compact TALEN variant” or “variant”         it is intended an endonuclease, rare-cutting endonuclease,         chimeric rare-cutting endonuclease, meganuclease, or compact         TALEN, enhanced compact TALEN, dual cleavage compact TALEN         obtained by replacement of at least one residue in the amino         acid sequence of the parent endonuclease, rare-cutting         endonuclease, chimeric rare-cutting endonuclease, meganuclease         or compact TALEN, enhanced compact TALEN, dual cleavage compact         TALEN with at least a different amino acid. “Variant”         designation also applies for instance for an enhanced compact         TALEN comprising at least one supplementary protein domain         (catalytic or enhancer domain) in comparison to the starting         compact TALEN entity. Are also encompassed in the scope of the         present definition, variants and protein domains comprised in         these variants which present a sequence with high percentage of         identity or high percentage of homology with sequences of         compact TALENs, enhanced compact TALENs, dual-cleavage compact         TALENs or protein domains and polypeptides according to the         present invention, at nucleotidic or polypeptidic levels. By         high percentage of identity or high percentage of homology it is         intended 60%, more preferably 70%, more preferably 75%, more         preferably 80%, more preferably 85%, more preferably 90%, more         preferably 95, more preferably 97%, more preferably 99% or any         integer comprised between 60% and 99%.     -   by “peptide linker”, “peptidic linker” or “peptide spacer” it is         intended to mean a peptide sequence which allows the connection         of different monomers in a fusion protein and the adoption of         the correct conformation for said fusion protein activity and         which does not alter the specificity of either of the monomers         for their targets. Peptide linkers can be of various sizes, from         3 amino acids to 50 amino acids as a non limiting indicative         range. Peptide linkers can also be structured or unstructured.     -   by “related to”, particularly in the expression “one cell type         related to the chosen cell type or organism”, is intended a cell         type or an organism sharing characteristics with said chosen         cell type or said chosen organism; this cell type or organism         related to the chosen cell type or organism, can be derived from         said chosen cell type or organism or not.     -   by “subdomain” it is intended the region of a LAGLIDADG homing         endonuclease core domain which interacts with a distinct part of         a homing endonuclease DNA target half-site.     -   by “targeting DNA construct/minimal repair matrix/repair matrix”         it is intended to mean a DNA construct comprising a first and         second portion that are homologous to regions 5′ and 3′ of the         DNA target in situ. The DNA construct also comprises a third         portion positioned between the first and second portion which         comprise some homology with the corresponding DNA sequence in         situ or alternatively comprise no homology with the regions 5′         and 3′ of the DNA target in situ. Following cleavage of the DNA         target, a homologous recombination event is stimulated between         the genome containing the targeted gene comprised in the locus         of interest and the repair matrix, wherein the genomic sequence         containing the DNA target is replaced by the third portion of         the repair matrix and a variable part of the first and second         portions of the repair matrix.     -   by “functional variant” is intended a catalytically active         variant of a protein, such variant can have additional         properties compared to its parent protein. As a non-limiting         example, a functional variant of a meganuclease can be able to         cleave a DNA target sequence, preferably said target being a new         target which is not cleaved by the parent meganuclease. This         definition also applies to compact TALENs, enhanced compact         TALENs, dual-cleavage compact TALENs or protein domains that         constitute such TALENs according to the present invention. Are         also encompassed in the scope of the present definition,         functional variants, polypeptides and protein domains comprised         in these molecules which present a sequence with high percentage         of identity or high percentage of homology with sequences of         compact TALENs, enhanced compact TALENs, dual-cleavage compact         TALENs or protein domains and polypeptides according to the         present invention, at nucleotidic or polypeptidic levels. By         high percentage of identity or high percentage of homology it is         intended 60%, more preferably 70%, more preferably 75%, more         preferably 80%, more preferably 85%, more preferably 90%, more         preferably 95, more preferably 97%, more preferably 99% or any         integer comprised between 60% and 99%.     -   by “derived from” or “derivative(s)” it is intended to mean for         instance a meganuclease variant which is created from a parent         meganuclease and hence the peptide sequence of the meganuclease         variant is related to (primary sequence level) but derived from         (mutations) the peptide sequence of the parent meganuclease. In         this definition, mutations encompass deletions or insertions of         several amino acid residues; as non-limiting example, a         truncated variant of an I-CreI meganuclease is considered as a         scaffold derived from I-CreI meganuclease. This expression can         also apply to compact TALENs, enhanced compact TALENs,         dual-cleavage compact TALENs or protein domains that constitute         such TALENs according to the present invention. Are also         encompassed in the scope of the present definition, derivatives         of compact TALENs, enhanced compact TALENs, dual-cleavage         compact TALENs or protein domains and derivatives of         polypeptides according to the present invention which present a         sequence with high percentage of identity or high percentage of         homology with sequences of compact TALENs, enhanced compact         TALENs, dual-cleavage compact TALENs or protein domains and         polypeptides according to the present invention, at nucleotidic         or polypeptidic levels. By high percentage of identity or high         percentage of homology it is intended 60%, more preferably 70%,         more preferably 75%, more preferably 80%, more preferably 85%,         more preferably 90%, more preferably 95, more preferably 97%,         more preferably 99% or any integer comprised between 60% and         99%.     -   by “I-CreI” is intended the wild-type I-CreI having the sequence         of pdb accession code 1g9y, corresponding to the sequence SEQ ID         NO: 1 in the sequence listing. In the present patent         application, I-CreI variants described can comprise an         additional Alanine after the first Methionine of the wild type         I-CreI sequence (SEQ ID NO: 1). These variants may also comprise         two additional Alanine residues and an Aspartic Acid residue         after the final Proline of the wild type I-CreI sequence as         shown in SEQ ID NO: 106. These additional residues do not affect         the properties of the enzyme and to avoid confusion these         additional residues do not affect the numeration of the residues         in I-CreI or a variant referred in the present patent         application, as these references exclusively refer to residues         of the wild type I-CreI enzyme (SEQ ID NO: 1) as present in the         variant, so for instance residue 2 of I-CreI is in fact residue         3 of a variant which comprises an additional Alanine after the         first Methionine.     -   by compact TALEN, enhanced compact TALEN, dual-cleavage compact         TALEN with novel specificity is intended a variant of these         proteins having a pattern of cleaved targets different from that         of their respective parent compact TALENs, enhanced compact         TALENs, dual-cleavage compact TALENs. The terms “novel         specificity”, “modified specificity”, “novel cleavage         specificity”, “novel substrate specificity” which are equivalent         and used indifferently, refer to the specificity of the variant         towards the nucleotides of the DNA target sequence.     -   by “I-CreI site” is intended a 22 to 24 bp double-stranded DNA         sequence which is cleaved by I-CreI. I-CreI sites include the         wild-type non-palindromic I-CreI homing site and the derived         palindromic sequences such as the sequence         5′-t⁻¹²c⁻¹¹a⁻¹⁰a⁻⁹a⁻⁸a⁻⁷c⁻⁶g⁻⁵t⁻⁴c⁻³g⁻²t⁻¹a₊₁c₊₂g₊₃a₊₄c₊₅g₊₆t₊₇t₊₈t₊₉t₊₁₀g₊₁₁a₊₁₂         (SEQ ID NO: 2), also called C1221 or C1221 target.     -   by “domain” or “core domain” is intended the “LAGLIDADG homing         endonuclease core domain” which is the characteristic 413413a         fold of the homing endonucleases of the LAGLIDADG family,         corresponding to a sequence of about one hundred amino acid         residues. Said domain comprises four beta-strands (β₁β₂β₃β₄)         folded in an anti-parallel beta-sheet which interacts with one         half of the DNA target. This domain is able to associate with         another LAGLIDADG homing endonuclease core domain which         interacts with the other half of the DNA target to form a         functional endonuclease able to cleave said DNA target. For         example, in the case of the dimeric homing endonuclease I-CreI         (163 amino acids), the LAGLIDADG homing endonuclease core domain         corresponds to the residues 6 to 94.     -   by “beta-hairpin” is intended two consecutive beta-strands of         the antiparallel beta-sheet of a LAGLIDADG homing endonuclease         core domain (β₁β₂ or β₃β₄) which are connected by a loop or a         turn.     -   by “single-chain meganuclease”, “single-chain chimeric         meganuclease”, “single-chain meganuclease derivative”,         “single-chain chimeric mega nuclease derivative” or         “single-chain derivative” is intended a meganuclease comprising         two LAGLIDADG homing endonuclease domains or core domains linked         by a peptidic spacer. The single-chain meganuclease is able to         cleave a chimeric DNA target sequence comprising one different         half of each parent meganuclease target sequence.     -   by “DNA target”, “DNA target sequence”, “target DNA sequence”,         “target sequence”, “target-site”, “target”, “site”, “site of         interest”, “recognition site”, “polynucleotide recognition         site”, “recognition sequence”, “homing recognition site”,         “homing site”, “cleavage site” is intended a double-stranded         palindromic, partially palindromic (pseudo-palindromic) or         non-palindromic polynucleotide sequence that is recognized and         can be cleaved by a LAGLIDADG homing endonuclease such as         I-CreI, or a variant, or a single-chain chimeric meganuclease         derived from I-CreI. Said DNA target sequence can be qualified         as “cleavable” by an endonuclease, rare-cutting endonuclease,         chimeric rare-cutting endonuclease or meganuclease when         recognized within a genomic sequence and known to correspond to         the DNA target sequence of a given endonuclease, rare-cutting         endonuclease, chimeric rare-cutting endonuclease or meganuclease         or a variant of such endonuclease, rare-cutting endonuclease,         chimeric rare-cutting endonuclease or meganuclease. These terms         refer to a specific DNA location, preferably a genomic location,         but also a portion of genetic material that can exist         independently to the main body of genetic material such as         plasmids, episomes, virus, transposons or in organelles such as         mitochondria or chloroplasts as non-limiting examples, at which         a double stranded break (cleavage) can be induced by the         endonuclease, rare-cutting endonuclease, chimeric rare-cutting         endonuclease or meganuclease. For the LAGLIDADG subfamily of         rare-cutting endonucleases, the DNA target is defined by the 5′         to 3′ sequence of one strand of the double-stranded         polynucleotide, as indicate above for C1221 (SEQ ID NO: 2).         Cleavage of the DNA target can occur at the nucleotides at         positions +2 and −2, respectively for the sense and the         antisense strand. Unless otherwise indicated, the position at         which cleavage of the DNA target by an I-CreI-derived variant         can occur, corresponds to the cleavage site on the sense strand         of the DNA target. In the particular case of compact TALENs, a         subclass of chimeric rare-cutting endonucleases, the following         expressions “DNA target”, “DNA target sequence”, “target DNA         sequence”, “target sequence”, “target-site”, “target”, “site”,         “site of interest”, “recognition site”, “polynucleotide         recognition site”, and “recognition sequence” can apply to         qualify their specific DNA target sequence with the         particularity that said specific DNA target sequence recognized         by the compact TALEN according to the invention is the one or         not that is processed and/or cut by the compact TALEN. A compact         TALEN, an enhanced compact TALEN or a dual cleavage compact         TALEN according to the present invention can process and/or cut         DNA within said specific DNA target sequence. A compact TALEN,         an enhanced compact TALEN or a dual cleavage compact TALEN can         also process and/or cut DNA outside said specific DNA target         sequence.     -   By “DNA nearby said specific DNA target sequence” or by “DNA         nearby” is intended DNA sequence or sequences located within or         outside said specific DNA target sequence. Are also intended DNA         sequence or sequences bound by a compact TALEN or an enhanced         compact TALEN at said specific DNA target sequence location or         DNA located at a 5′ or 3′ distance of 1-100 base pairs (bps),         1-50 base pairs (bps) or 1-25 base pairs (bps) from said         specific DNA target sequence.

When several compact TALENs have to be used in a particular genome engineering application, DNA target sequence for each compact TALENs of the combination to be used can be located on a same endogenous genomic DNA locus of interest or not. Said DNA target sequences can be located at an approximative distance of 1-1000 base pairs (bps), more preferably 1-500 bps, more preferably 1-100 bps, more preferably 1-100 bps, more preferably 1-50 bps, more preferably 1-25 bps, more preferably 1-10 bps. In another embodiment, said DNA target sequence for each compact TALENs of the combination to be used can be located on the same DNA strand or not. Said DNA target sequences located at distances mentioned above are “nearby” DNA sequences in reference to the target DNA sequence for DNA processing according to the present invention.

-   -   by “single double-stranded DNA target sequence” is intended a         compact-TALEN or enhanced compact TALEN or dual-cleavage compact         TALEN binding site. The recognition DNA binding site of a         compact-TALEN or enhanced compact TALEN or dual-cleavage compact         TALEN can be ranging from 12 to 100 base pairs (bp) in length,         usually greater than 12 bps in length.     -   by “DNA target half-site”, “half cleavage site” or half-site” is         intended the portion of the DNA target which is bound by each         LAGLIDADG homing endonuclease core domain.     -   The term “endonuclease” refers to any wild-type or variant         enzyme capable of catalyzing the hydrolysis (cleavage) of bonds         between nucleic acids within a DNA or RNA molecule, preferably a         DNA molecule. Endonucleases can be classified as rare-cutting         endonucleases when having typically a polynucleotide recognition         greater than 12 base pairs (bp) in length, more preferably of         14-45 bp. Rare-cutting endonucleases significantly increase HR         by inducing DNA double-strand breaks (DSBs) at a defined locus         (Rouet, Smih et al. 1994; Rouet, Smih et al. 1994; Choulika,         Perrin et al. 1995; Pingoud and Silva 2007). Rare-cutting         endonucleases can for example be a homing endonuclease (Paques         and Duchateau 2007), a chimeric Zinc-Finger nuclease (ZFN)         resulting from the fusion of engineered zinc-finger domains with         the catalytic domain of a restriction enzyme such as FokI         (Porteus and Carroll 2005) or a chemical endonuclease         (Eisenschmidt, Lanio et al. 2005; Arimondo, Thomas et al. 2006;         Simon, Cannata et al. 2008). In chemical endonucleases, a         chemical or peptidic cleaver is conjugated either to a polymer         of nucleic acids or to another DNA recognizing a specific target         sequence, thereby targeting the cleavage activity to a specific         sequence. Chemical endonucleases also encompass synthetic         nucleases like conjugates of orthophenanthroline, a DNA cleaving         molecule, and triplex-forming oligonucleotides (TFOs), known to         bind specific DNA sequences (Kalish and Glazer 2005). Such         chemical endonucleases are comprised in the term “endonuclease”         according to the present invention.

Rare-cutting endonucleases can also be for example TALENs, a new class of chimeric nucleases using a FokI catalytic domain and a DNA binding domain derived from Transcription Activator Like Effector (TALE), a family of proteins used in the infection process by plant pathogens of the Xanthomonas genus (Boch, Scholze et al. 2009; Boch, Scholze et al. 2009; Moscou and Bogdanove 2009; Moscou and Bogdanove 2009; Christian, Cermak et al. 2010; Christian, Cermak et al. 2010; Li, Huang et al. 2010; Li, Huang et al. 2011). The functional layout of a FokI-based TALE-nuclease (TALEN) is essentially that of a ZFN, with the Zinc-finger DNA binding domain being replaced by the TALE domain. As such, DNA cleavage by a TALEN requires two DNA recognition regions flanking an unspecific central region. Rare-cutting endonucleases encompassed in the present invention can also be derived from TALENs. The authors of the present invention have developed a new type of TALENs that can be engineered to specifically recognize and process target DNA efficiently. These novel “compact TALENs” (cTALENs) do not require dimerization for DNA processing activity, thereby alleviating the need for “dual” target sites with intervening DNA “spacers”; these compact TALENs can be seen as one subclass of rare-cutting endonucleases or chimeric rare-cutting endonucleases according to the present invention.

Rare-cutting endonuclease can be a homing endonuclease, also known under the name of meganuclease. Such homing endonucleases are well-known to the art (Stoddard 2005). Homing endonucleases recognize a DNA target sequence and generate a single- or double-strand break. Homing endonucleases are highly specific, recognizing DNA target sites ranging from 12 to 45 base pairs (bp) in length, usually ranging from 14 to 40 bp in length. The homing endonuclease according to the invention may for example correspond to a LAGLIDADG endonuclease, to a HNH endonuclease, or to a GIY-YIG endonuclease.

In the wild, meganucleases are essentially represented by homing endonucleases. Homing Endonucleases (HEs) are a widespread family of natural meganucleases including hundreds of proteins families (Chevalier and Stoddard 2001). These proteins are encoded by mobile genetic elements which propagate by a process called “homing”: the endonuclease cleaves a cognate allele from which the mobile element is absent, thereby stimulating a homologous recombination event that duplicates the mobile DNA into the recipient locus. Given their exceptional cleavage properties in terms of efficacy and specificity, they could represent ideal scaffolds to derive novel, highly specific endonucleases.

HEs belong to four major families. The LAGLIDADG family, named after a conserved peptidic motif involved in the catalytic center, is the most widespread and the best characterized group. Seven structures are now available. Whereas most proteins from this family are monomeric and display two LAGLIDADG motifs, a few have only one motif, and thus dimerize to cleave palindromic or pseudo-palindromic target sequences.

Although the LAGLIDADG peptide is the only conserved region among members of the family, these proteins share a very similar architecture. The catalytic core is flanked by two DNA-binding domains with a perfect two-fold symmetry for homodimers such as I-CreI (Chevalier, Monnat et al. 2001), I-MsoI (Chevalier, Turmel et al. 2003) and I-CeuI (Spiegel, Chevalier et al. 2006) and with a pseudo symmetry for monomers such as I-SceI (Moure, Gimble et al. 2003), I-DmoI (Silva, Dalgaard et al. 1999) or I-AniI (Bolduc, Spiegel et al. 2003). Both monomers and both domains (for monomeric proteins) contribute to the catalytic core, organized around divalent cations. Just above the catalytic core, the two LAGLIDADG peptides also play an essential role in the dimerization interface. DNA binding depends on two typical saddle-shaped αββαββα folds, sitting on the DNA major groove. Other domains can be found, for example in inteins such as PI-PfuI (Ichiyanagi, Ishino et al. 2000) and PI-SceI (Moure, Gimble et al. 2002), whose protein splicing domain is also involved in DNA binding.

The making of functional chimeric meganucleases, by fusing the N-terminal I-DmoI domain with an I-CreI monomer (Chevalier, Kortemme et al. 2002; Epinat, Arnould et al. 2003); International PCT Application WO 03/078619 (Cellectis) and WO 2004/031346 (Fred Hutchinson Cancer Research Center, Stoddard et al)) have demonstrated the plasticity of LAGLIDADG proteins.

Different groups have also used a semi-rational approach to locally alter the specificity of the I-CreI (Seligman, Stephens et al. 1997; Sussman, Chadsey et al. 2004); International PCT Applications WO 2006/097784, WO 2006/097853, WO 2007/060495 and WO 2007/049156 (Cellectis); (Arnould, Chames et al. 2006; Rosen, Morrison et al. 2006; Smith, Grizot et al. 2006), I-SceI (Doyon, Pattanayak et al. 2006), PI-SceI (Gimble, Moure et al. 2003) and I-MsoI (Ashworth, Havranek et al. 2006).

In addition, hundreds of I-CreI derivatives with locally altered specificity were engineered by combining the semi-rational approach and High Throughput Screening:

-   -   Residues Q44, R68 and R70 or Q44, R68, D75 and 177 of I-CreI         were mutagenized and a collection of variants with altered         specificity at positions±3 to 5 of the DNA target (5NNN DNA         target) were identified by screening (International PCT         Applications WO 2006/097784 and WO 2006/097853 (Cellectis);         (Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).     -   Residues K28, N30 and Q38 or N30, Y33 and Q38 or K28, Y33, Q38         and S40 of I-CreI were mutagenized and a collection of variants         with altered specificity at positions ±8 to 10 of the DNA target         (10NNN DNA target) were identified by screening (Arnould, Chames         et al. 2006; Smith, Grizot et al. 2006); International PCT         Applications WO 2007/060495 and WO 2007/049156 (Cellectis)).

Two different variants were combined and assembled in a functional heterodimeric endonuclease able to cleave a chimeric target resulting from the fusion of two different halves of each variant DNA target sequence ((Arnould, Chames et al. 2006; Smith, Grizot et al. 2006); International PCT Applications WO 2006/097854 and WO 2007/034262).

Furthermore, residues 28 to 40 and 44 to 77 of I-CreI were shown to form two partially separable functional subdomains, able to bind distinct parts of a homing endonuclease target half-site (Smith, Grizot et al. 2006); International PCT Applications WO 2007/049095 and WO 2007/057781 (Cellectis)).

The combination of mutations from the two subdomains of I-CreI within the same monomer allowed the design of novel chimeric molecules (homodimers) able to cleave a palindromic combined DNA target sequence comprising the nucleotides at positions ±3 to 5 and ±8 to 10 which are bound by each subdomain ((Smith, Grizot et al. 2006); International PCT Applications WO 2007/049095 and WO 2007/057781 (Cellectis)).

The method for producing meganuclease variants and the assays based on cleavage-induced recombination in mammal or yeast cells, which are used for screening variants with altered specificity are described in the International PCT Application WO 2004/067736; (Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006). These assays result in a functional LacZ reporter gene which can be monitored by standard methods.

The combination of the two former steps allows a larger combinatorial approach, involving four different subdomains. The different subdomains can be modified separately and combined to obtain an entirely redesigned meganuclease variant (heterodimer or single-chain molecule) with chosen specificity. In a first step, couples of novel meganucleases are combined in new molecules (“half-meganucleases”) cleaving palindromic targets derived from the target one wants to cleave. Then, the combination of such “half-meganucleases” can result in a heterodimeric species cleaving the target of interest. The assembly of four sets of mutations into heterodimeric endonucleases cleaving a model target sequence or a sequence from different genes has been described in the following Cellectis International patent applications: XPC gene (WO2007/093918), RAG gene (WO2008/010093), HPRT gene (WO2008/059382), beta-2 microglobulin gene (WO2008/102274), Rosa26 gene (WO2008/152523), Human hemoglobin beta gene (WO2009/13622) and Human interleukin-2 receptor gamma chain gene (WO2009019614).

These variants can be used to cleave genuine chromosomal sequences and have paved the way for novel perspectives in several fields, including gene therapy.

Examples of such endonuclease include I-Sce I, I-Chu I, I-Cre I, I-Csm I, PI-Sce I, PI-Tli I, PI-Mtu I, I-Ceu I, I-Sce II, I-Sce III, HO, PI-Civ I, PI-Ctr I, PI-Aae I, PI-Bsu I, PI-Dha I, PI-Dra I, PI-May I, PI-Mch I, PI-Mfu PI-MfI I, PI-Mga I, PI-Mgo I, PI-Min I, PI-Mka I, PI-Mle I, PI-Mma I, PI-Msh I, PI-Msm I, PI-Mth I, PI-Mtu I, PI-Mxe I, PI-Npu I, PI-Pfu I, PI-Rma I, PI-Spb I, PI-Ssp I, PI-Fac I, PI-Mja I, PI-Pho I, PI-Tag I, PI-Thy I, PI-Tko I, PI-Tsp I, I-MsoI.

A homing endonuclease can be a LAGLIDADG endonuclease such as I-SceI, I-CreI, I-CeuI, I-MsoI, and I-DmoI.

Said LAGLIDADG endonuclease can be I-Sce I, a member of the family that contains two LAGLIDADG motifs and functions as a monomer, its molecular mass being approximately twice the mass of other family members like I-CreI which contains only one LAGLIDADG motif and functions as homodimers.

Endonucleases mentioned in the present application encompass both wild-type (naturally-occurring) and variant endonucleases. Endonucleases according to the invention can be a “variant” endonuclease, i.e. an endonuclease that does not naturally exist in nature and that is obtained by genetic engineering or by random mutagenesis, i.e. an engineered endonuclease. This variant endonuclease can for example be obtained by substitution of at least one residue in the amino acid sequence of a wild-type, naturally-occurring, endonuclease with a different amino acid. Said substitution(s) can for example be introduced by site-directed mutagenesis and/or by random mutagenesis. In the frame of the present invention, such variant endonucleases remain functional, i.e. they retain the capacity of recognizing (binding function) and optionally specifically cleaving a target sequence to initiate gene targeting process.

The variant endonuclease according to the invention cleaves a target sequence that is different from the target sequence of the corresponding wild-type endonuclease. Methods for obtaining such variant endonucleases with novel specificities are well-known in the art.

Endonucleases variants may be homodimers (meganuclease comprising two identical monomers) or heterodimers (meganuclease comprising two non-identical monomers). It is understood that the scope of the present invention also encompasses endonuclease variants per se, including heterodimers (WO2006097854), obligate heterodimers (WO2008093249) and single chain meganucleases (WO03078619 and WO2009095793) as non limiting examples, able to cleave one target of interest in a polynucleotidic sequence or in a genome. The invention also encompasses hybrid variant per se composed of two monomers from different origins (WO03078619).

Endonucleases with novel specificities can be used in the method according to the present invention for gene targeting and thereby integrating a transgene of interest into a genome at a predetermined location.

-   -   by “parent meganuclease” it is intended to mean a wild type         meganuclease or a variant of such a wild type meganuclease with         identical properties or alternatively a meganuclease with some         altered characteristics in comparison to a wild type version of         the same meganuclease. This expression can also be transposed to         an endonuclease, a rare-cutting endonuclease, a chimeric         rare-cutting endonuclease, a TALEN or a compact TALEN and         derivatives.     -   By “delivery vector” or “delivery vectors” is intended any         delivery vector which can be used in the present invention to         put into cell contact (i.e. “contacting”) or deliver inside         cells or subcellular compartments agents/chemicals and molecules         (proteins or nucleic acids) needed in the present invention. It         includes, but is not limited to liposomal delivery vectors,         viral delivery vectors, drug delivery vectors, chemical         carriers, polymeric carriers, lipoplexes, polyplexes,         dendrimers, microbubbles (ultrasound contrast agents),         nanoparticles, emulsions or other appropriate transfer vectors.         These delivery vectors allow delivery of molecules, chemicals,         macromolecules (genes, proteins), or other vectors such as         plasmids, peptides developed by Diatos. In these cases, delivery         vectors are molecule carriers. By “delivery vector” or “delivery         vectors” is also intended delivery methods to perform         transfection.     -   The terms “vector” or “vectors” refer to a nucleic acid molecule         capable of transporting another nucleic acid to which it has         been linked. A “vector” in the present invention includes, but         is not limited to, a viral vector, a plasmid, a RNA vector or a         linear or circular DNA or RNA molecule which may consists of a         chromosomal, non chromosomal, semi-synthetic or synthetic         nucleic acids. Preferred vectors are those capable of autonomous         replication (episomal vector) and/or expression of nucleic acids         to which they are linked (expression vectors). Large numbers of         suitable vectors are known to those of skill in the art and         commercially available.

Viral vectors include retrovirus, adenovirus, parvovirus (e.g. adenoassociated viruses), coronavirus, negative strand RNA viruses such as orthomyxovirus (e.g., influenza virus), rhabdovirus (e.g., rabies and vesicular stomatitis virus), paramyxovirus (e.g. measles and Sendai), positive strand RNA viruses such as picornavirus and alphavirus, and double-stranded DNA viruses including adenovirus, herpesvirus (e.g., Herpes Simplex virus types 1 and 2, Epstein-Barr virus, cytomegalovirus), and poxvirus (e.g., vaccinia, fowlpox and canarypox). Other viruses include Norwalk virus, togavirus, flavivirus, reoviruses, papovavirus, hepadnavirus, and hepatitis virus, for example. Examples of retroviruses include: avian leukosis-sarcoma, mammalian C-type, B-type viruses, D type viruses, HTLV-BLV group, lentivirus, spumavirus (Coffin, J. M., Retroviridae: The viruses and their replication, In Fundamental Virology, Third Edition, B. N. Fields, et al., Eds., Lippincott-Raven Publishers, Philadelphia, 1996).

-   -   By “lentiviral vector” is meant HIV-Based lentiviral vectors         that are very promising for gene delivery because of their         relatively large packaging capacity, reduced immunogenicity and         their ability to stably transduce with high efficiency a large         range of different cell types. Lentiviral vectors are usually         generated following transient transfection of three (packaging,         envelope and transfer) or more plasmids into producer cells.         Like HIV, lentiviral vectors enter the target cell through the         interaction of viral surface glycoproteins with receptors on the         cell surface. On entry, the viral RNA undergoes reverse         transcription, which is mediated by the viral reverse         transcriptase complex. The product of reverse transcription is a         double-stranded linear viral DNA, which is the substrate for         viral integration in the DNA of infected cells.     -   By “integrative lentiviral vectors (or LV)”, is meant such         vectors as non limiting example, that are able to integrate the         genome of a target cell.     -   At the opposite by “non integrative lentiviral vectors (or         NILV)” is meant efficient gene delivery vectors that do not         integrate the genome of a target cell through the action of the         virus integrase.

One type of preferred vector is an episome, i.e., a nucleic acid capable of extra-chromosomal replication. Preferred vectors are those capable of autonomous replication and/or expression of nucleic acids to which they are linked. Vectors capable of directing the expression of genes to which they are operatively linked are referred to herein as “expression vectors. A vector according to the present invention comprises, but is not limited to, a YAC (yeast artificial chromosome), a BAC (bacterial artificial), a baculovirus vector, a phage, a phagemid, a cosmid, a viral vector, a plasmid, a RNA vector or a linear or circular DNA or RNA molecule which may consist of chromosomal, non chromosomal, semi-synthetic or synthetic DNA. In general, expression vectors of utility in recombinant DNA techniques are often in the form of “plasmids” which refer generally to circular double stranded DNA loops which, in their vector form are not bound to the chromosome. Large numbers of suitable vectors are known to those of skill in the art. Vectors can comprise selectable markers, for example: neomycin phosphotransferase, histidinol dehydrogenase, dihydrofolate reductase, hygromycin phosphotransferase, herpes simplex virus thymidine kinase, adenosine deaminase, glutamine synthetase, and hypoxanthine-guanine phosphoribosyl transferase for eukaryotic cell culture; TRP1 for S. cerevisiae; tetracyclin, rifampicin or ampicillin resistance in E. coli. Preferably said vectors are expression vectors, wherein a sequence encoding a polypeptide of interest is placed under control of appropriate transcriptional and translational control elements to permit production or synthesis of said polypeptide. Therefore, said polynucleotide is comprised in an expression cassette. More particularly, the vector comprises a replication origin, a promoter operatively linked to said encoding polynucleotide, a ribosome binding site, a RNA-splicing site (when genomic DNA is used), a polyadenylation site and a transcription termination site. It also can comprise an enhancer or silencer elements. Selection of the promoter will depend upon the cell in which the polypeptide is expressed. Suitable promoters include tissue specific and/or inducible promoters. Examples of inducible promoters are: eukaryotic metallothionine promoter which is induced by increased levels of heavy metals, prokaryotic lacZ promoter which is induced in response to isopropyl-β-D-thiogalacto-pyranoside (IPTG) and eukaryotic heat shock promoter which is induced by increased temperature. Examples of tissue specific promoters are skeletal muscle creatine kinase, prostate-specific antigen (PSA), α-antitrypsin protease, human surfactant (SP) A and B proteins, β-casein and acidic whey protein genes.

Inducible promoters may be induced by pathogens or stress, more preferably by stress like cold, heat, UV light, or high ionic concentrations (reviewed in Potenza C et al. 2004, In vitro Cell Dev Biol 40:1-22). Inducible promoter may be induced by chemicals (reviewed in (Moore, Samalova et al. 2006); (Padidam 2003); (Wang, Zhou et al. 2003); (Zuo and Chua 2000).

Delivery vectors and vectors can be associated or combined with any cellular permeabilization techniques such as sonoporation or electroporation or derivatives of these techniques.

-   -   By cell or cells is intended any prokaryotic or eukaryotic         living cells, cell lines derived from these organisms for in         vitro cultures, primary cells from animal or plant origin.     -   By “primary cell” or “primary cells” are intended cells taken         directly from living tissue (i.e. biopsy material) and         established for growth in vitro, that have undergone very few         population doublings and are therefore more representative of         the main functional components and characteristics of tissues         from which they are derived from, in comparison to continuous         tumorigenic or artificially immortalized cell lines. These cells         thus represent a more valuable model to the in vivo state they         refer to.     -   In the frame of the present invention, “eukaryotic cells” refer         to a fungal, plant or animal cell or a cell line derived from         the organisms listed below and established for in vitro culture.

More preferably, the fungus is of the genus Aspergillus, Penicillium, Acremonium, Trichoderma, Chrysoporium, Mortierella, Kluyveromyces or Pichia; More preferably, the fungus is of the species Aspergillus niger, Aspergillus nidulans, Aspergillus oryzae, Aspergillus terreus, Penicillium chrysogenum, Penicillium citrinum, Acremonium Chrysogenum, Trichoderma reesei, Mortierella alpine, Chrysosporium lucknowense, Kluyveromyces lactis, Pichia pastoris or Pichia ciferrii.

More preferably the plant is of the genus Arabidospis, Nicotiana, Solanum, lactuca, Brassica, Oryza, Asparagus, Pisum, Medicago, Zea, Hordeum, Secale, Triticum, Capsicum, Cucumis, Cucurbita, Citrullis, Citrus, Sorghum; More preferably, the plant is of the species Arabidospis thaliana, Nicotiana tabaccum, Solanum lycopersicum, Solanum tuberosum, Solanum melongena, Solanum esculentum, Lactuca saliva, Brassica napus, Brassica oleracea, Brassica rapa, Oryza glaberrima, Oryza sativa, Asparagus officinalis, Pisum sativum, Medicago sativa, zea mays, Hordeum vulgare, Secale cereal, Triticum aestivum, Triticum durum, Capsicum sativus, Cucurbita pepo, Citrullus lanatus, Cucumis melo, Citrus aurantifolia, Citrus maxima, Citrus medica, Citrus reticulata.

More preferably the animal cell is of the genus Homo, Rattus, Mus, Sus, Bos, Danio, Canis, Felis, Equus, Salmo, Oncorhynchus, Gallus, Meleagris, Drosophila, Caenorhabditis; more preferably, the animal cell is of the species Homo sapiens, Rattus norvegicus, Mus musculus, Sus scrofa, Bos taurus, Danio rerio, Canis lupus, Felis catus, Equus caballus, Salmo salar, Oncorhynchus mykiss, Gallus gallus, Meleagris gallopavo, Drosophila melanogaster, Caenorhabditis elegans.

In the present invention, the cell can be a plant cell, a mammalian cell, a fish cell, an insect cell or cell lines derived from these organisms for in vitro cultures or primary cells taken directly from living tissue and established for in vitro culture. As non-limiting examples, cell can be protoplasts obtained from plant organisms listed above. As non limiting examples cell lines can be selected from the group consisting of CHO-K1 cells; HEK293 cells; Caco2 cells; U2-OS cells; NIH 3T3 cells; NSO cells; SP2 cells; CHO-S cells; DG44 cells; K-562 cells, U-937 cells; MRCS cells; IMR90 cells; Jurkat cells; HepG2 cells; HeLa cells; HT-1080 cells; HCT-116 cells; Hu-h7 cells; Huvec cells; Molt 4 cells.

All these cell lines can be modified by the method of the present invention to provide cell line models to produce, express, quantify, detect, study a gene or a protein of interest; these models can also be used to screen biologically active molecules of interest in research and production and various fields such as chemical, biofuels, therapeutics and agronomy as non-limiting examples. Adoptive immunotherapy using genetically engineered T cells is a promising approach for the treatment of malignancies and infectious diseases. Most current approaches rely on gene transfer by random integration of an appropriate T Cell Receptor (TCR) or Chimeric Antigen Receptor (CAR). Targeted approach using rare-cutting endonucleases is an efficient and safe alternative method to transfer genes into T cells and generate genetically engineered T cells.

-   -   by “homologous” is intended a sequence with enough identity to         another one to lead to homologous recombination between         sequences, more particularly having at least 95% identity,         preferably 97% identity and more preferably 99%.     -   “identity” refers to sequence identity between two nucleic acid         molecules or polypeptides. Identity can be determined by         comparing a position in each sequence which may be aligned for         purposes of comparison. When a position in the compared sequence         is occupied by the same base, then the molecules are identical         at that position. A degree of similarity or identity between         nucleic acid or amino acid sequences is a function of the number         of identical or matching nucleotides at positions shared by the         nucleic acid sequences. Various alignment algorithms and/or         programs may be used to calculate the identity between two         sequences, including FASTA, or BLAST which are available as a         part of the GCG sequence analysis package (University of         Wisconsin, Madison, Wis.), and can be used with, e.g., default         setting.     -   by “mutation” is intended the substitution, deletion, insertion         of one or more nucleotides/amino acids in a polynucleotide         (cDNA, gene) or a polypeptide sequence. Said mutation can affect         the coding sequence of a gene or its regulatory sequence. It may         also affect the structure of the genomic sequence or the         structure/stability of the encoded mRNA.     -   In the frame of the present invention, the expression         “double-strand break-induced mutagenesis” (DSB-induced         mutagenesis) refers to a mutagenesis event consecutive to an         NHEJ event following an endonuclease-induced DSB, leading to         insertion/deletion at the cleavage site of an endonuclease.     -   By “gene” is meant the basic unit of heredity, consisting of a         segment of DNA arranged in a linear manner along a chromosome,         which codes for a specific protein or segment of protein. A gene         typically includes a promoter, a 5′ untranslated region, one or         more coding sequences (exons), optionally introns, a 3′         untranslated region. The gene may further comprise a terminator,         enhancers and/or silencers.     -   As used herein, the term “transgene” refers to a sequence         encoding a polypeptide. Preferably, the polypeptide encoded by         the transgene is either not expressed, or expressed but not         biologically active, in the cell, tissue or individual in which         the transgene is inserted. Most preferably, the transgene         encodes a therapeutic polypeptide useful for the treatment of an         individual.     -   The term “gene of interest” or “GOI” refers to any nucleotide         sequence encoding a known or putative gene product.     -   As used herein, the term “locus” is the specific physical         location of a DNA sequence (e.g. of a gene) on a chromosome. The         term “locus” usually refers to the specific physical location of         an endonuclease's target sequence on a chromosome. Such a locus,         which comprises a target sequence that is recognized and cleaved         by an endonuclease according to the invention, is referred to as         “locus according to the invention”. Also, the expression         “genomic locus of interest” is used to qualify a nucleic acid         sequence in a genome that can be a putative target for a         double-strand break according to the invention. It is understood         that the considered genomic locus of interest of the present         invention can not only qualify a nucleic acid sequence that         exists in the main body of genetic material (i.e. in a         chromosome) of a cell but also a portion of genetic material         that can exist independently to said main body of genetic         material such as plasmids, episomes, virus, transposons or in         organelles such as mitochondria or chloroplasts as non-limiting         examples.     -   By the expression “loss of genetic information” is understood         the elimination or addition of at least one given DNA fragment         (at least one nucleotide) or sequence, bordering the recognition         sites of the endonucleases, chimeric rare-cutting endonucleases,         compact TALEN or enhanced compact TALEN of the present invention         or the intervening sequence between at least two processing         sites of the endonucleases, chimeric rare-cutting endonucleases,         compact TALEN or enhanced compact TALEN of the present invention         and leading to a change of the original sequence around said         endonuclease-cutting sites, chimeric rare-cutting         endonuclease-cutting sites, compact TALEN or enhanced compact         TALEN recognition DNA binding site within the genomic locus of         interest. This loss of genetic information can be, as a         non-limiting example, the elimination of an intervening sequence         between two endonuclease-cutting sitesor between two processing         sites of a compact TALEN or enhanced compact TALEN. As another         non-limiting example, this loss of genetic information can also         be an excision of a single-strand of DNA spanning the binding         region of a compact TALEN or an enhanced compact TALEN according         to the present invention     -   By “scarless re-ligation” or “scarless religation” is intended         the perfect re-ligation event, without loss of genetic         information (no insertion/deletion events) of the DNA broken         ends through NHEJ process after the creation of a double-strand         break event.     -   By “Imprecise NHEJ” is intended the re-ligation of nucleic acid         ends generated by a DSB, with insertions or deletions of         nucleotides. Imprecise NHEJ is an outcome and not a repair         pathway and can result from different NHEJ pathways (Ku         dependent or Ku independent as non-limiting examples).     -   By “fusion protein” is intended the result of a well-known         process in the art consisting in the joining of two or more         genes which originally encode for separate proteins or part of         them, the translation of said “fusion gene” resulting in a         single polypeptide with functional properties derived from each         of the original proteins.     -   By “chimeric rare-cutting endonuclease” is meant any fusion         protein comprising a rare-cutting endonuclease. Said         rare-cutting endonuclease might be at the N-terminal part of         said chimeric rare-cutting endonuclease; at the opposite, said         rare-cutting endonuclease might be at the C-terminal part of         said chimeric rare-cutting endonuclease. A “chimeric         rare-cutting endonuclease” according to the present invention         which comprises two catalytic domains can be described as         “bi-functional” or as “bi-functional meganuclease”. A “chimeric         rare-cutting endonuclease” according to the present invention         which comprises more than two catalytic domains can be described         as “multi-functional” or as “multi-functional meganuclease”. As         non-limiting examples, chimeric rare-cutting endonucleases         according to the present invention can be a fusion protein         between a rare-cutting endonuclease and one catalytic domain;         chimeric rare-cutting endonucleases according to the present         invention can also be a fusion protein between a rare-cutting         endonuclease and two catalytic domains. As mentioned previously,         the rare-cutting endonuclease part of chimeric rare-cutting         endonucleases according to the present invention can be a         meganuclease comprising two identical monomers, two         non-identical monomers, or a single chain meganuclease. The         rare-cutting endonuclease part of chimeric rare-cutting         endonucleases according to the present invention can also be the         DNA-binding domain of an inactive rare-cutting endonuclease. In         other non-limiting examples, chimeric rare-cutting endonucleases         according to the present invention can be derived from a         TALE-nuclease (TALEN), i.e. a fusion between a DNA-binding         domain derived from a Transcription Activator Like Effector         (TALE) and one or two catalytic domains. In other non-limiting         examples, a subclass of chimeric rare-cutting endonucleases         according to the present invention can be a “compact         TALE-nuclease” (cTALEN), i.e. a fusion between an engineered         core TALE scaffold comprising at least a Repeat Variable         Dipeptide regions domain and at least one catalytic domain, said         fusion protein constituting a compact TALEN active entity that         does not require dimerization for DNA processing activity. Said         catalytic domain can be an endonuclease as listed in table 2 as         non-limiting examples; said catalytic domain can be a         frequent-cutting endonuclease such as a restriction enzyme         selected from the group consisting of MmeI, R-HinPII, R.MspI,         R.MvaI, Nb.BsrDI, BsrDI A, Nt.BspD6I, ss.BspD6I, R.PleI, MlyI         and AlwI as non-limiting restriction enzymes examples listed in         table 2.     -   By “enhancer domain(s)” or “enhancer(s)” are meant protein         domains that provide functional and/or structural support to a         protein scaffold, a compact TALEN as a non-limiting example,         therefore allowing an enhancement in global DNA processing         efficiency of the resulting fusion protein, i.e. an enhanced         compact TALEN, relative to the DNA processing efficiency of the         starting compact TALEN. A particular domain is an enhancer         domain when it provides at least a 5% enhancement in efficiency         of the starting scaffold, more preferably 10%, again more         preferably 15%, again more preferably 20%, again more preferably         25%, again more preferably 50%, again more preferably greater         than 50%. Non-limiting examples of such enhancer domains are         given in Tables 1 and 2. By “auxiliary enhancer domains” or         “auxiliary enhancers” or “auxiliary domains” are meant protein         domains acting in trans with a compact TALEN or an enhanced         compact TALEN to provide an additional function that is not         essential for said basic compact TALEN activity or said enhanced         compact TALEN activity. When such auxiliary enhancers are used,         compact TALEN or enhanced compact TALEN are converted to “trans         TALEN”, respectively trans compact TALEN and trans enhanced         compact TALEN.

By “catalytic domain” is intended the protein domain or module of an enzyme containing the active site of said enzyme; by active site is intended the part of said enzyme at which catalysis of the substrate occurs. Enzymes, but also their catalytic domains, are classified and named according to the reaction they catalyze. The Enzyme Commission number (EC number) is a numerical classification scheme for enzymes, based on the chemical reactions they catalyze (www.chem.qmul.ac.uk). In the scope of the present invention, any catalytic domain can be fused to an engineered core TALE scaffold to generate a compact TALEN active entity with a DNA processing efficiency provided by at least said catalytic domain activity. Said catalytic domain can provide a nuclease activity (endonuclease or exonuclease activities, cleavase or nickase), a polymerase activity, a kinase activity, a phosphatase activity, a methylase activity, a topoisomerase activity, an integrase activity, a transposase activity or a ligase activity as non-limiting examples. Non-limiting examples of such catalytic domains are given in Tables 1 and 2. In a preferred embodiment of the present invention, said catalytic domain can be considered as an enhancer domain. If catalytically active, said enhancer domain can provide functional and/or structural support to the compact TALEN scaffold leading to an enhanced compact TALEN when fused to it. If catalytically inactive, said enhancer domain provides structural support to compact TALEN scaffold leading to an enhanced compact TALEN when fused to it. It can be envisioned from the present invention to fuse catalytic domains according to the present invention to one part of a classical TALEN in order to give these classical TALENs new catalytical properties provided by at least said catalytic domain activity or to improve their DNA processing efficiency.

-   -   By “nuclease catalytic domain” is intended the protein domain         comprising the active site of an endonuclease or an exonuclease         enzyme. Such nuclease catalytic domain can be, for instance, a         “cleavase domain” or a “nickase domain”. By “cleavase domain” is         intended a protein domain whose catalytic activity generates a         Double Strand Break (DSB) in a DNA target. By “nickase domain”         is intended a protein domain whose catalytic activity generates         a single strand break in a DNA target sequence. Non-limiting         examples of such catalytic domains are given in Tables 1 and 2         with a GenBank or NCBI or UniProtKB/Swiss-Prot number as a         reference.     -   By a “TALE-nuclease” (TALEN) or a “classical TALEN” is intended         a fusion protein consisting of a DNA-binding domain derived from         a Transcription Activator Like Effector (TALE) and one FokI         catalytic domain, that need to dimerize to form an active entity         able to cleave a DNA target sequence.     -   By “compact TALE-nuclease” (cTALEN) is intended a general         designation according to the present invention for a fusion         protein between an engineered core TALE scaffold comprising at         least one Repeat Variable Dipeptides domain and at least one         catalytic domain, said fusion protein constituting a compact         TALEN (or cTALEN) active entity and not requiring dimerization         for DNA processing activity. Compact TALENs are designed to         alleviate the need for multiple independent protein moieties         when targeting a DNA cleavage event. Importantly, the requisite         “spacer” region and dual target sites essential for the function         of current TALENs are unnecessary. In other words, the compact         TALEN according to the present invention is an active entity         unit able, by itself, to target only one specific single         double-stranded DNA target sequence of interest through one DNA         binding domain and to process DNA nearby said single         double-stranded DNA target sequence of interest. In addition,         since the catalytic domain does not require specific DNA         contact, there are no restrictions on regions surrounding the         core TALE DNA binding domain. In the scope of the present         invention, it can be also envisioned some sequence preference in         the catalytic domain. When a cTALEN comprises only one catalytic         domain, cTALEN can be qualified as a “basic cTALEN” or “cTALEN”.         When a cTALEN further comprises at least one “enhancer domain”,         cTALEN can be qualified as an enhanced cTALEN or an “eTALEN”. A         cTALEN or an eTALEN that comprise at least one cleavase         catalytic domain and one nickase catalytic domain or at least         two cleavase catalytic domains can be specifically qualified as         a dual-cleavage cTALEN or a “dcTALEN”. A cTALEN or an eTALEN         acting with an auxiliary domain in trans is qualified as a trans         compact TALEN or a trans enhanced compact TALEN, both being         “trans TALEN”.

The above written description of the invention provides a manner and process of making and using it such that any person skilled in this art is enabled to make and use the same, this enablement being provided in particular for the subject matter of the appended claims, which make up a part of the original description.

As used above, the phrases “selected from the group consisting of,” “chosen from,” and the like include mixtures of the specified materials.

Where a numerical limit or range is stated herein, the endpoints are included. Also, all values and subranges within a numerical limit or range are specifically included as if explicitly written out.

The above description is presented to enable a person skilled in the art to make and use the invention, and is provided in the context of a particular application and its requirements. Various modifications to the preferred embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments and applications without departing from the spirit and scope of the invention. Thus, this invention is not intended to be limited to the embodiments shown, but is to be accorded the widest scope consistent with the principles and features disclosed herein.

Having generally described this invention, a further understanding can be obtained by reference to certain specific examples, which are provided herein for purposes of illustration only, and are not intended to be limiting unless otherwise specified.

EXAMPLES Example 1

The wild-type I-CreI meganuclease (SEQ ID NO: 106) was chosen as the parent scaffold on which to fuse the catalytic domain of I-TevI (SEQ ID NO: 107). Wild-type I-TevI functions as a monomeric cleavase of the GIY-YIG family to generate a staggered double-strand break in its target DNA. Guided by biochemical and structural data, variable length constructs were designed from the N-terminal region of 1-TevI that encompass the entire catalytic domain and deletion-intolerant region of its linker (SEQ ID NO: 109 to SEQ ID NO: 114). In all but one case, fragments were fused to the N-terminus of I-CreI with an intervening 5-residue polypeptide linker (-QGPSG-; SEQ ID NO: 103). The linker-less fusion construct naturally contained residues (-LGPDGRKA-; SEQ ID NO: 104) similar to those in the artificial linker. As I-CreI is a homodimer, all fusion constructs contain three catalytic centers (FIG. 4, where “catalytic domain”=cleavase): the natural I-CreI active site at the interface of the dimer and one I-TevI active site per monomer.

The activity of each “tri-functional” meganuclease was assessed using our yeast assay previously described in International PCT Applications WO 2004/067736 and in (Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006). All constructs were able to cleave the C1221 target DNA with an activity comparable to that of wild-type I-CreI (Table 4). To validate the activity of the I-TevI catalytic domain independent of the I-CreI catalytic core, D20N point mutants were made to inactivate the I-CreI scaffold [SEQ ID NO: 108, SEQ ID NO: 115 to SEQ ID NO: 120; Chevalier, Sussman et al. 2004)]. Tests in our yeast assays showed no visible activity from the inactivated I-CreI (D20N) mutant protein alone (Table 4). However, cleavage activity could be observed for fusions having the I-TevI catalytic domain (Table 4).

TABLE 4 Activity in Yeast assay for I-TevI/I-CreI fusions. The relative activity of wild-type and fusion proteins on the two parent protein targets (C1221 for I-CreI and Tev for I-TevI) is shown. Maximal activity (++++) is seen with each given protein on its native DNA target. I-CreI_N20 is an inactive variant of the wild-type I-CreI scaffold. In all other cases, activity is only detected on the C1221 target since DNA recognition is driven by the I-CreI scaffold. The “N20” fusion variants illustrate cleavage activity due to the I-TevI catalytic domain. Relative Activity in Yeast Assay (37° C.) Protein Construct C1221 Target Tev Target I-CreI ++++ − I-TevI − ++++ I-CreI_N20 − − hTevCre_D01 ++++ − hTevCre_D02 ++++ − hTevCre_D03 ++++ − hTevCre_D04 ++++ − hTevCre_D05 ++++ − hTevCre_D06 ++++ − hTevCre_D01_N20 ++ − hTevCre_D02_N20 ++ − hTevCre_D03_N20 ++ − hTevCre_D04_N20 ++ − hTevCre_D05_N20 − − hTevCre_D06_N20 − − Relative activity is scaled as: −, no activity detectable; +, <25% activity; ++, 25% to <50% activity; +++, 50% to <75% activity; ++++, 75% to 100% activity.

Example 2

Protein-fusion scaffolds were designed based on a truncated form of I-CreI (SEQ ID NO: 106, I-CreI_X: SEQ ID NO: 121) and three different linker polypeptides (NFS1=SEQ ID NO: 98; NFS2=SEQ ID NO: 99; CFS1=SEQ ID NO: 100) fused to either the N- or C-terminus of the protein. Structure models were generated in all cases, with the goal of designing a “baseline” fusion linker that would traverse the I-CreI parent scaffold surface with little to no effect on its DNA binding or cleavage activities. For the two N-terminal fusion scaffolds, the polypeptide spanning residues 2 to 153 of I-CreI was used, with a K82A mutation to allow for linker placement. The C-terminal fusion scaffold contains residues 2 to 155 of wild-type I-CreI. For both fusion scaffold types, the “free” end of the linker (i.e. onto which a polypeptide can be linked) is designed to be proximal to the DNA, as determined from models built using the I-CreI/DNA complex structures as a starting point (PDB id: 1g9z). The two I-CreI N-terminal fusion scaffolds (1-CreI_NFS1=SEQ ID NO: 122 and I-CreI_NFS2=SEQ ID NO: 123) and the single C-terminal fusion scaffold (1-CreI_CFS1=SEQ ID NO: 124) were tested in our yeast assay (see Example 1) and found to have activity similar to that of wild-type I-CreI (Table 5).

TABLE 5 Activity in Yeast assay for ColE7/I-CreI fusions. The relative activity of wild-type and fusion proteins on theC1221 target is shown. I-CreI_X represents a truncated version of I-CreI based on the crystal structure and was used as the foundation for the fusion scaffolds (I-CreI_NFS1, I-CreI_NFS2 and I-CreI_CFS1). “N20” constructs are inactive variants of the respective I-CreI-based scaffolds. Activity is detected in all cases wherein the I-CreI scaffold is active or when DNA catalysis is provided by the ColE7 domain. Relative Activity in Yeast Assay (37° C.) Protein Construct C1221 Target I-CreI ++++ I-CreI_X ++++ I-CreI_NFS1 ++++ I-CreI_NFS2 ++++ I-CreI_CFS1 ++++ I-CreI_NFS1_N20 − I-CreI_NFS2_N20 − I-CreI_CFS1_N20 − hColE7Cre_D0101 ++++ hColE7Cre_D0102 ++++ hCreColE7_D0101 ++++ hColE7Cre_D0101_N20 +++ hColE7Cre_D0102_N20 +++ hCreColE7_D0101_N20 ++ Relative activity is scaled as: −, no activity detectable; +, <25% activity; ++, 25% to <50% activity; +++, 50% to <75% activity; ++++, 75% to 100% activity.

Colicin E7 is a non-specific nuclease of the HNH family able to process single- and double-stranded DNA (Hsia, Chak et al. 2004). Guided by biochemical and structural data, the region of ColE7 that encompasses the entire catalytic domain (SEQ ID NO: 140; (Hsia, Chak et al. 2004) was selected. This ColE7 domain was fused to the N-terminus of either I-CreI_NFS1 (SEQ ID NO: 122) or I-CreI_NFS2 (SEQ ID NO: 123) to create hColE7Cre_D0101 (SEQ ID NO: 128) or hColE7Cre_D0102 (SEQ ID NO: 129), respectively. In addition, a C-terminal fusion construct, hCreColE7_D0101 (SEQ ID NO: 130), was generated using I-CreI_CFS1 (SEQ ID NO: 124). As I-CreI is a homodimer, all fusion constructs contain three catalytic centers (FIG. 4, where “catalytic domain”=cleavage): the natural I-CreI active site at the interface of the dimer and one ColE7 active site per monomer.

The activity of each “tri-functional” meganuclease was assessed using our yeast assay (see Example 1). All constructs were able to cleave the C1221 target DNA with an activity comparable to that of wild-type I-CreI (Table 5).

To validate the activity of the ColE7 catalytic domain independent of the I-CreI catalytic core, D20N point mutants were made to inactivate the I-CreI scaffold (SEQ ID NO: 125, SEQ ID NO: 126, SEQ ID NO: 127, SEQ ID NO: 131, SEQ ID NO: 132, SEQ ID NO: 133; (Chevalier, Sussman et al. 2004)). Tests in our yeast assays showed no visible activity from the inactivated I-CreI (D20N) mutant proteins alone (Table 5). However, cleavage activity could be observed for fusions having the ColE7 catalytic domain (Table 5).

Example 3

Two core TALE scaffolds are generated onto which (a) different sets of RVD domains could be inserted to change DNA binding specificity, and; (b) a selection of catalytic domains could be attached, N- or C-terminal, to effect DNA cleavage (or nicking). The core scaffolds (sT1: SEQ ID NO: 134 and sT2: SEQ ID NO: 135) differ in the N- and C-terminal regions, where sT2 is a truncated variant lacking 152 amino acid residues from the N-terminus (Szurek, Rossier et al. 2002) and the last 220 residues from the C-terminus compared to sT1. In sT1, the C-terminal region is a truncation with respect to wild-type TALE domains, ending at a fortuitously defined restriction site (BamHI) in the DNA coding sequence.

Using the two core scaffolds, four “baseline” TALE DNA binding proteins (bT1-Avr=SEQ ID NO: 136, bT2-Avr=SEQ ID NO: 137, bT1-Pth ═SEQ ID NO 138 and bT2-Pth ═SEQ ID NO 139) are generated by insertion of the corresponding set of repeat domains that recognize the naturally occurring asymmetric sequences AvrBs3 (19 bp) and PthXo1 (25 bp) (FIG. 3). Example protein sequences of the baseline scaffolds are listed in SEQ ID NO: 136 to SEQ ID NO: 139. As is, these scaffolds can be tested in vitro for DNA binding ability on targets having only a single recognition sequence. For comparison with existing TALENs, the catalytic domain of the FokI nuclease (SEQ ID NO: 368 and particularly residues P381 to F583 as non-limiting example) can be fused to either the N- or C-terminus of the baseline scaffolds. Effective cleavage using these controls requires target site DNAs that contain two TALE binding sequences.

In addition to verifying activity using naturally occurring sequences, five artificial RVD constructs recognizing relevant sequences were generated (FIG. 3): RagT2-R, NptIIT5-L, NptIIT5-R, NptIIT6-L, NptIIT6-R. Example protein sequences of the insert RVDs are listed in SEQ ID NO: 253 to SEQ ID NO: 257. Artificial RVD sequences are used as noted above within the sT1 or sT2 scaffold to generate the desired targeted compact TALENs.

Basic compact TALENs (cTALENs) are generated via fusion of catalytic domains to either the N- or C-terminus of the baseline scaffolds (FIG. 5, A or B, respectively). A non-exhaustive list of catalytic domains amenable to fusion with TALE DNA binding domains is presented in Table 2. A non-exhaustive list of linkers that can be used is presented in Table 3. It is notable that linker design can depend on the nature of the catalytic domain attached and its given application. It can also be anticipated that specially engineered linkers can be constructed to better control or regulate the activity of either or both domains. Examples 5, 6 and 7 below discuss additional and alternative methods in which linkers can be defined. All cTALEN designs are assessed using our yeast assay (see Example 1) and provide detectable activity comparable to existing engineered meganucleases.

Example 3a TALE::TevI Compact TALEN

The catalytic domain of I-TevI (SEQ ID NO: 20), a member of the GIY-YIG endonuclease family, was fused to a TALE-derived scaffold (composed of a N-terminal domain, a central core composed of RVDs and a C-terminal domain) to create a new class of cTALEN (TALE::TevI). To distinguish the orientation (N-terminal vs. C-terminal) of the catalytic domain (CD) fusions, construct names are written as either CD::TALE-RVD (catalytic domain is fused N-terminal to the TALE domain) or TALE-RVD::CD (catalytic domain is fused C-terminal to the TALE domain), where “-RVD” optionally designates the sequence recognized by the TALE domain and “CD” is the catalytic domain type. Herein, we describe novel TALE::TevI constructions that target AvrBs3 sequence for example, thus named TALE-AvrBs3::TevI.

Activity of TALE::TevI in Yeast

A core TALE scaffold, sT2 (SEQ ID NO: 135), was selected onto which (a) different sets of RVD domains could be inserted to change DNA binding specificity, and; (b) a selection of I-TevI-derived catalytic domains could be attached, N- or C-terminal, to effect DNA cleavage (or nicking). The previously mentioned sT2 truncated scaffold was generated by the PCR from a full-length core TALEN scaffold template (pCLS7183, SEQ ID NO: 141) using primers CMP_G061 (SEQ ID NO: 142) and CMP_G065 (SEQ ID NO: 143) and was cloned into vector pCLS7865 (SEQ ID NO: 144) to generate pCLS7865-cTAL11_CFS1 (pCLS9009, SEQ ID NO: 145), where CFS1 designates the amino acid sequence -GSSG- (with underlying restriction sites BamHI and Kpn21 in the coding DNA to facilitate cloning, SEQ ID NO: 468). Three variants of the I-TevI (SEQ ID NO: 20) catalytic domain were amplified by the PCR on templates TevCreD01 [SEQ ID NO: 109 protein in plasmid pCLS6614 (SEQ ID NO: 146)] using the primer pair CMP_G069 (SEQ ID NO: 147) and CMP_G070 (SEQ ID NO: 148), TevCreD02 [SEQ ID NO: 110 protein in plasmid pCLS6615 (SEQ ID NO: 203)] using the primer pair CMP_G069 (SEQ ID NO: 147) and CMP_G071 (SEQ ID NO: 149) or TevCreD05 [SEQ ID NO: 113 protein in plasmid pCLS6618 (SEQ ID NO: 258)] using the primer pair CMP_G069 (SEQ ID NO: 147) and CMP_G115 (SEQ ID NO: 259) and subcloned into the pCLS9009 backbone by restriction and ligation using BamHI and EagI restriction sites, yielding pCLS7865-cT11_TevD01 (pCLS9010, SEQ ID NO: 150), pCLS7865-cT11_TevD02 (pCLS9011, SEQ ID NO: 151) and pCLS7865-cT11_TevD05 (pCLS15775, SEQ ID NO: 260), respectively. All fusions contain the dipeptide -GS- linking the TALE-derived DNA binding domain and I-TevI-derived catalytic domain.

The DNA sequence coding for the RVDs to target the AvrBs3 site (SEQ ID NO: 152) was subcloned into both plasmids pCLS9010 (SEQ ID NO: 150, encoding the protein of SEQ ID NO: 420), pCLS9011 (SEQ ID NO: 151, encoding the protein of SEQ ID NO: 421) and pCLS15775 (SEQ ID NO: 260, encoding the protein of SEQ ID NO: 422) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TALE-AvrBs3::TevI constructs cT11AvrTevD01 (pCLS9012, SEQ ID NO: 218, encoding the protein of SEQ ID NO: 423), cT11Avr_TevD02 (pCLS9013, SEQ ID NO: 153, encoding the protein of SEQ ID NO: 424) and cT11Avr_TevD05 (pCLS15776, SEQ ID NO: 261, encoding the protein of SEQ ID NO: 425), respectively. These TALE-AvrBs3::TevI constructs were sequenced and the insert transferred to additional vectors as needed (see below).

The final TALE-AvrBs3::TevI yeast expression plasmids, pCLS8523 (SEQ ID NO: 154), pCLS8524 (SEQ ID NO: 155) and pCLS12092 (SEQ ID NO: 262), were prepared by yeast in vivo cloning using plasmids pCLS9012, pCLS9013 and pCLS15776, respectively. To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of each plasmid linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform, respectively, the yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::TevI constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21). TALE-AvrBs3::TevI activity levels on their respective targets in yeast cells are shown on FIG. 9. Data summarized in FIG. 9 show that TALE-AvrBs3::TevI is active against several targets in Yeast.

Activity of TALE::TevI in Mammalian Cells

DNA encoding the TALE-AvrBs3::TevI construct from either pCLS9012 (SEQ ID NO: 218) or pCLS9013 (SEQ ID NO: 153) was subcloned into the pCLS1853 (SEQ ID NO: 193) mammalian expression plasmid using Ascl and XhoI restriction enzymes for the receiving plasmid and BssHII and XhoI restriction enzymes for the TALE-AvrBs3::TevI insert, leading to the mammalian expression plasmids pCLS8993 and pCLS8994 (SEQ ID NO: 194 and 195), respectively.

All mammalian target reporter plasmids containing the TALEN DNA target sequences were constructed using the standard Gateway protocol (INVITROGEN) into a CHO reporter vector (Arnould, Chames et al. 2006, Grizot, Epinat et al. 2010). The TALE-AvrBs3::TevI constructs were tested in an extrachromosomal assay in mammalian cells (CHO K1) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN, which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21).

For this assay, CHO K1 cells were transfected in a 96-well plate format with 75 ng of target vector and an increasing quantity of each variant DNA from 0.7 to 25 ng, in the presence of PolyFect reagent NIL per well). The total amount of transfected DNA was completed to 125 ng (target DNA, variant DNA, carrier DNA) using an empty vector. Seventy-two hours after transfection, culture medium was removed and 150 μl of lysis/revelation buffer for β-galactosidase liquid assay was added. After incubation at 37° C., optical density was measured at 420 nm. The entire process is performed on an automated Velocityll BioCel platform (Grizot, Epinat et al. 2009).

Activity levels in mammalian cells for the TALE-AvrBs3::TevI constructs (12.5 ng DNA transfected) on the Avr15 target (SEQ ID NO: 167) are shown in FIG. 10. TALE-AvrBs3::TevI appears to be efficient to cleave the target sequence.

TALE::TevI Nickase Activity

The results described in examples above illustrate two TALE::TevI fusions, each containing one TALE-based DNA binding domain and one I-TevI-based catalytic domain, working to generate detectable activity. The assays used measure tandem repeat recombination by single-strand annealing, a process that is triggered essentially by a DSB (Sugawara and Haber 1992; Paques and Duchateau 2007). TALE::TevI fusions can have a nickase activity insufficient to alone trigger a signal in the cell-based assay. However, two TALE::TevI proteins binding on two nearby sites can sometimes generate two independent nicks, that when proximal and on different DNA strands can create a DSB. In this case, each TALE::TevI is a cTALEN able to generate a nick.

Different experiments are set up to measure TALE::TevI nickase activity:

Super-Coiled Circular Plasmid Nicking and/or Linearization Assay

The sequences encoding the TALE-AvrBs3::TevI constructs cT11Avr_TevD01 and cT11Avr_TevD02 are cloned into a T7-based expression vector using NcoI/EagI restriction sites to yield plasmids pCLS9021 (SEQ ID NO: 201) and pCLS9022 (SEQ ID NO: 202), respectively. This cloning step results in TALE-AvrBs3::TevI proteins having an additional hexa-His tag for purification. Plasmids pCLS9021 and pCLS9022 are then used to produce active proteins by one of two methods:

-   -   1. Plasmids are used in a standard in vitro         transcription/translation system; lysates from the translation         are used directly without further purification.     -   2. Plasmids are used to transform E. coli BL21(DE3) cells for         expression using standard protocols, namely: growth to log         phase, induction with IPTG, harvest, cell lysis and purification         via affinity methods for His-tagged proteins.         Active proteins are assayed against DNA targets having either         none, one or two AvrBs3 recognition site sequences. When more         than one site is present, identical recognition sequences are         juxtaposed with the 3′ ends proximal and separated by “spacer”         DNA ranging from 5 to 40 bps.

A super-coiled circular plasmid nicking and/or linearization assay is performed. Plasmids harboring the DNA targets described above are prepared by standard methods and column purified to yield super-coiled plasmid of >98% purity. Increasing amounts of TALE-AvrBs3::TevI proteins (prepared as described above) are incubated with each plasmid under conditions to promote DNA cleavage for 1 h at 37° C. Reaction products are separated on agarose gels and visualized by EtBr staining.

Linear DNA Nicking and/or Cleavage Assay

A linear DNA nicking and/or cleavage assay is also performed. PCR products containing the target sequences described above are prepared by standard methods and column purified to yield linear substrate of >98% purity. Increasing amounts of TALE-AvrBs3::TevI proteins (prepared as described above) are then incubated with each PCR substrate under conditions to promote DNA cleavage for 1 h at 37° C. Reaction products are separated on a denaturing acrylamide gel and the single-strand DNA visualized.

Engineering of the TALE::TevI

Variants differing by truncations of the C-terminal domain of the AvrBs3-derived TALEN (SEQ ID NO: 196) are chosen as starting scaffolds. A subset of these variants includes truncation after positions E886 (C0), P897 (C11), G914 (C28), L926 (C40), D950 (C64), R1000 (C115), D1059 (C172) (the protein domains of truncated C-terminal domains C11 to C172 are respectively given in SEQ ID NO: 204 to 209) and P1117 [also referred as Cter wt or WT Cter (SEQ ID NO: 210) lacking the activation domain of the C-terminal domain of natural AvrBs3 (SEQ ID NO: 220)]. The plasmids coding for the variant scaffolds containing the AvrBs3-derived N-terminal domain, the AvrBs3-derived set of repeat domains and the truncated AvrBs3-derived C-terminal domain [pCLS7821, pCLS7803, pCLS7807, pCLS7809, pCLS7811, pCLS7813, pCLS7817 (SEQ ID NO: 211 to 217) which are based on the pCLS7184 (SEQ ID NO: 196)] allow cloning of any catalytic domain in fusion to the C-terminal domain, using the restriction sites BamHI and EagI.

Variants of the catalytic domain of I-TevI (SEQ ID NO: 20) are designed from the N-terminal region of I-TevI. A subset of these variants includes truncations of the catalytic domain, as the deletion-intolerant region of its linker, the deletion-tolerant region of its linker and its zinc finger (SEQ ID NO: 197 to 200) named in Liu et al, 2008 (Liu, Dansereau et al. 2008).

The DNA corresponding to these variants of I-TevI is amplified by the PCR to introduce, at the DNA level, a BamHI (at the 5′ of the coding strand) and a EagI (at the 3′ of the coding strand) restriction site and, at the protein level, a linker (for example -SGGSGS- stretch, SEQ ID NO: 219) between the C terminal domain of the TALE and the variant of the catalytic domain of I-TevI. The final TALE::TevI constructs are generated by insertion of the variant of I-TevI catalytic domains into the scaffold variants using BamHI and EagI and standard molecular biology procedures.

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::TevI constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21).

Example 3b TevI::TALE Compact TALEN

The sT2 (SEQ ID NO: 135) core TALE scaffold described in example 3a was selected to generate pCLS7865-cTAL11_NFS1 (pCLS9008, SEQ ID NO: 234), where NFS1 designates the amino acid sequence -GSSG- (SEQ ID NO: 468) (with underlying restriction sites BamHI and Kpn21 in the coding DNA to facilitate cloning). Four variants of the I-TevI (SEQ ID NO: 20) catalytic domain were amplified by the PCR on templates TevCreD01 [SEQ ID NO: 109 protein in plasmid pCLS6614 (SEQ ID NO: 146)] using the primer pairs CMP_G001 (SEQ ID NO: 239) and CMP_G067 (SEQ ID NO: 263) or CMP_G152 (SEQ ID NO: 264), TevCreD02 [SEQ ID NO: 110 protein in plasmid pCLS6615 (SEQ ID NO: 203)] using the primer pair CMP_G001 (SEQ ID NO: 239) and CMP_G068 (SEQ ID NO: 240) or TevCreD05 [SEQ ID NO: 113 protein in plasmid pCLS6618 (SEQ ID NO: 258)] using the primer pair CMP_G001 (SEQ ID NO: 239) and CMP_G114 (SEQ ID NO: 265) and subcloned into the pCLS9008 backbone by restriction and ligation using NcoI and Kpn2I restriction sites, yielding pCLS7865-TevW01_cT11 (pCLS15777, SEQ ID NO: 266, encoding the protein of SEQ ID NO: 426), pCLS7865-TevD01_cT11 (pCLS15778, SEQ ID NO: 267, encoding the protein of SEQ ID NO: 427), pCLS7865-TevD02_cT11 (pCLS12730, SEQ ID NO: 235, encoding the protein of SEQ ID NO: 428) and pCLS7865-TevD05_cT11 (pCLS15779, SEQ ID NO: 268, encoding the protein of SEQ ID NO: 429), respectively. Whereas the TevW01_cT11-based fusion contains the dipeptide -SG- linking the TALE-derived DNA binding domain and I-TevI-derived catalytic domain, all others constructs incorporate a longer pentapeptide -QGPSG- (SEQ ID NO: 469) to link the domains.

Activity of TevI::TALE in Yeast

The DNA sequence coding for the RVDs to target the AvrBs3 site (SEQ ID NO: 152) was subcloned into plasmids pCLS15777 (SEQ ID NO: 266), pCLS15778 (SEQ ID NO: 267) and pCLS12730 (SEQ ID NO: 235) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TevI::TALE-AvrBs3 constructs TevW01_cT11Avr (pCLS15780, SEQ ID NO: 269, encoding the protein of SEQ ID NO: 430), TevD01_cT11Avr (pCLS15781, SEQ ID NO: 270, encoding the protein of SEQ ID NO: 431) and TevD02_cT11Avr (pCLS12731, SEQ ID NO: 236, encoding the protein of SEQ ID NO: 432), respectively. A similar cloning technique was used to introduce the RVDs to target the RagT2-R site (SEQ ID NO: 271) into plasmid pCLS15779 (SEQ ID NO: 268) to create the subsequent construct TevD05_cT11RagT2-R (pCLS15782, SEQ ID NO: 272). All TevI::TALE constructs were sequenced and the inserts transferred to additional vectors as needed (see below).

The final TevI::TALE-based yeast expression plasmids, pCLS11979 (SEQ ID NO: 273), pCLS8521 (SEQ ID NO: 274), pCLS8522 (SEQ ID NO: 237) and pCLS12100 (SEQ ID NO: 275), were prepared by yeast in vivo cloning using plasmid pCLS15780 (SEQ ID NO: 269), pCLS15781 (SEQ ID NO: 270), pCLS12731 (SEQ ID NO: 236) and pCLS15782 (SEQ ID NO: 272), respectively. To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of each plasmid linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform, respectively, the yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TevI::TALE-AvrBs3 and TevI::TALE-RagT2-R constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21). In addition, constructs were tested on a target having only a single AvrBs3 or RagT2-R recognition site (SEQ ID NO: 238, Table 8). The TevI::TALE-AvrBs3 activity level in yeast was comparable to that of TALE-AvrBs3::TevI (pCLS8524, SEQ ID NO: 155) on suitable targets. Significant activity is illustrated in table 8 for a sample single-site target, according to the cTALEN of the present invention.

TABLE 8 Activity of TevI::TALE-AvrBs3 and and TevI::TALE- RagT2-R on dual- and single-site DNA targets. TALEN Construct TevI:: TevI:: TALE- TALE- TALE- AvrBs3:: Target DNA AvrBs3 RagT2-R FokI Avr25 (dual-site) ++++ n.d. ++++ (SEQ ID NO: 177) Avr25RAGT2R ++ ++ n.d. (single-site) (SEQ ID NO: 238) Relative activity is scaled as: n.d., no activity detectable; +, <25% activity; ++, 25% to <50% activity; +++, 50% to <75% activity; ++++, 75% to 100% activity.

Activity of TevI::TALE in Plants

The DNA sequence coding for the RVDs to target the NptIIT5-L and NptIIT6-L sites (SEQ ID NO: 276 to 279) were subcloned into plasmid pCLS12730 (SEQ ID NO: 235) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequences to create the subsequent TevI::TALE constructs TevD02_cT11NptIIT5-L (pCLS15783, SEQ ID NO: 280) and TevD02_cT11NptIIT6-L (pCLS15784, SEQ ID NO: 281), respectively. The constructs were sequenced and the TevI::TALE inserts transferred by standard cloning techniques to plasmid pCLS14529 (SEQ ID NO: 282) to generate the final TevI::TALE-NptIIT5-L and TevI::TALE-NptIIT6-L expression plasmids, pCLS14579 (SEQ ID NO: 283) and pCLS14581 (SEQ ID NO: 284), respectively. Plasmid pCLS14529 allows for cloning gene of interest sequences downstream of a promoter that confers high levels of constitutive expression in plant cells.

To test activity in plant cells, a YFP-based single-strand annealing (SSA) assay was employed. The YFP reporter gene has a short duplication of coding sequence that is interrupted by either an NptIIT5 or NptIIT6 TALEN target site. Cleavage at the target site stimulates recombination between the repeats, resulting in reconstitution of a functional YFP gene. To quantify cleavage, the reporter is introduced along with a construct encoding a FokI-based TALEN or compact TALEN into tobacco protoplasts by PEG-mediated transformation (as known or derived from the state of the art). Uniform transformation efficiencies were obtained by using the same amount of plasmid in each transformation—i.e. 15 μg each of plasmids encoding YFP and either the TALEN or cTALEN. After 24 hours, the protoplasts were subjected to flow cytometry to quantify the number of YFP positive cells. The TevI::TALE activity levels, using cTALENs according to the present invention, in plants were comparable to those of a FokI-based TALEN control constructs on the targets tested (Table 9).

TABLE 9 Activity of TevI::TALE-NptIIT5-L and TevI::TALE- NptIIT6-L on appropriate DNA targets. TALEN Construct TevI:: TevI:: Target TALE- NptII5.1 TALE- NptII6.1 DNA NptIIT5-L control NptIIT6-L control NptII5.1 +++ + n.a. n.a. NptII6.1 n.a. n.a. + + Relative activity is scaled to the control constructs as: n.a., not applicable; +, 100% activity of control (2% YFP positive cells).

Example 3c TALE::NucA Compact TALEN

NucA (SEQ ID NO: 26), a nonspecific endonuclease from Anabaena sp., was fused to a TALE-derived scaffold (composed of a N-terminal domain, a central core composed of RVDs and a C-terminal domain) to create a new class of cTALEN (TALE::NucA). To distinguish the orientation (N-terminal vs. C-terminal) of the catalytic domain (CD) fusions, construct names are written as either CD::TALE-RVD (catalytic domain is fused N-terminal to the TALE domain) or TALE-RVD::CD (catalytic domain is fused C-terminal to the TALE domain), where “-RVD” optionally designates the sequence recognized by the TALE domain and “CD” is the catalytic domain type. Herein, we describe novel TALE::NucA constructions that target for example the AvrBs3 sequence, and are thus named TALE-AvrBs3::NucA. Notably, the wild-type NucA endonuclease can be inhibited by complex formation with the NuiA protein (SEQ ID NO: 229). In a compact TALEN context, the NuiA protein can function as an auxiliary domain to modulate the nuclease activity of TALE::NucA constructs.

Activity of TALE::NucA in Yeast

A core TALE scaffold, sT2 (SEQ ID NO: 135), was selected onto which (a) different sets of RVD domains could be inserted to change DNA binding specificity, and; (b) a selection of NucA-derived catalytic domains could be attached, N- or C-terminal, to effect DNA cleavage (or nicking). As previously mentioned, the sT2 truncated scaffold was generated by the PCR from a full-length core TALEN scaffold template (pCLS7183, SEQ ID NO: 141) using primers CMP_G061 (SEQ ID NO: 142) and CMP_G065 (SEQ ID NO: 143) and was cloned into vector pCLS7865 (SEQ ID NO: 144) to generate pCLS7865-cTAL11_CFS1 (pCLS9009, SEQ ID NO: 145), where CFS1 designates the amino acid sequence -GSSG- (SEQ ID NO: 468) (with underlying restriction sites BamHI and Kpn2I in the coding DNA to facilitate cloning). The NucA (SEQ ID NO: 26) catalytic domain, corresponding to amino acid residues 25 to 274, was subcloned into the pCLS9009 backbone (SEQ ID NO: 145) by restriction and ligation using BamHI and EagI restriction sites, yielding pCLS7865-cT11_NucA (pCLS9937, SEQ ID NO: 221, encoding the protein of SEQ ID NO: 433). The fusion contains the dipeptide -GS- linking the TALE-derived DNA binding domain and NucA-derived catalytic domain. The cloning step also brings at the amino acid level an AAD sequence at the Cter of the NucA catalytic domain.

The DNA sequence coding for the RVDs to target the AvrBs3 site (SEQ ID NO: 152) was subcloned into plasmid pCLS9937 (SEQ ID NO: 221) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TALE-AvrBs3::NucA construct cT11Avr_NucA (pCLS9938, SEQ ID NO: 222, encoding the protein of SEQ ID NO: 434). The TALE-AvrBs3::NucA construct was sequenced and the insert transferred to additional vectors as needed (see below).

The final TALE-AvrBs3::NucA yeast expression plasmid, pCLS9924 (SEQ ID NO: 223), was prepared by yeast in vivo cloning using plasmid pCLS9938 (SEQ ID NO: 222). To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of plasmid (pCLS9938) linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform the yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::NucA construct was tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224; FIG. 22).

Engineering of the TALE::NucA

Variants differing by truncations of the C-terminal domain of the AvrBs3-derived TALEN (SEQ ID NO: 196) are chosen as starting scaffolds. A subset of these variants includes truncation after positions E886 (C0), P897 (C11), G914 (C28), L926 (C40), D950 (C64), R1000 (C115), D1059 (C172) (the protein domains of truncated C-terminal domains C11 to C172 are respectively given in SEQ ID NO: 204 to 209) and P1117 [also referred as Cter wt or WT Cter (SEQ ID NO: 210) lacking the activation domain of the C-terminal domain of natural AvrBs3 (SEQ ID NO: 220)]. The plasmids coding for the variant scaffolds containing the AvrBs3-derived N-terminal domain, the AvrBs3-derived set of repeat domains and the truncated AvrBs3-derived C-terminal domain [pCLS7821, pCLS7803, pCLS7807, pCLS7809, pCLS7811, pCLS7813, pCLS7817 (SEQ ID NO: 211 to 217) which are based on the pCLS7184 (SEQ ID NO: 196)] allow cloning of any catalytic domain in fusion to the C-terminal domain, using the restriction sites BamHI and EagI.

The DNA corresponding to amino acid residues 25 to 274 of NucA is amplified by the PCR to introduce, at the DNA level, a BamHI (at the 5′ of the coding strand) and a EagI (at the 3′ of the coding strand) restriction site and, at the protein level, a linker (for example -SGGSGS- stretch, SEQ ID NO: 219) between the C terminal domain of the TALE and the NucA catalytic domain. The final TALE::NucA constructs are generated by insertion of the NucA catalytic domain into the scaffold variants using BamHI and EagI and standard molecular biology procedures. For example, scaffold variants truncated after positions P897 (C11), G914 (C28) and D950 (C64), respectively encoded by pCLS7803, pCLS7807, pCLS7811, (SEQ ID NO: 212, 213 and 215), were fused to the NucA catalytic domain (SEQ ID NO: 26), leading to pCLS9596, pCLS9597, and pCLS9599 (SEQ ID NO: 225 to 227). The cloning step also brings at the amino acid level an AAD sequence at the Cter of the NucA catalytic domain.

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::NucA constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, TALE-AvrBs3::NucA constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224). Data summarized in FIG. 11 show that TALE-AvrBs3::NucA constructs are active on all targets having at least one AvrBs3 recognition site, according to the cTALEN of the present invention.

Example 3d TALE::ColE7 Compact TALEN

The catalytic domain of ColE7 (SEQ ID NO: 140), a nonspecific endonuclease from E. coli, was fused to a TALE-derived scaffold (composed of a N-terminal domain, a central core composed of RVDs and a C-terminal domain) to create a new class of cTALEN (TALE::ColE7). To distinguish the orientation (N-terminal vs. C-terminal) of the catalytic domain (CD) fusions, construct names are written as either CD::TALE-RVD (catalytic domain is fused N-terminal to the TALE domain) or TALE-RVD::CD (catalytic domain is fused C-terminal to the TALE domain), where “-RVD” optionally designates the sequence recognized by the TALE domain and “CD” is the catalytic domain type. Herein, we describe novel TALE::ColE7 constructions that target for example the AvrBs3 sequence, and are thus named TALE-AvrBs3::ColE7. Notably, the wild-type ColE7 endonuclease can be inhibited by complex formation with the Im7 immunity protein (SEQ ID NO: 230). In a compact TALEN context, the Im7 protein can function as an auxiliary domain to modulate the nuclease activity of TALE::ColE7 constructs.

Activity of TALE::ColE7 in Yeast

A core TALE scaffold, sT2 (SEQ ID NO: 135), was selected onto which (a) different sets of RVD domains could be inserted to change DNA binding specificity, and; (b) a selection of ColE7-derived catalytic domains could be attached, N- or C-terminal, to effect DNA cleavage (or nicking). As previously mentioned, the sT2 truncated scaffold was generated by the PCR from a full-length core TALEN scaffold template (pCLS7183, SEQ ID NO: 141) using primers CMP_G061 (SEQ ID NO: 142) and CMP_G065 (SEQ ID NO: 143) and was cloned into vector pCLS7865 (SEQ ID NO: 144) to generate pCLS7865-cTAL11_CFS1 (pCLS9009, SEQ ID NO: 145), where CFS1 designates the amino acid sequence -GSSG- (SEQ ID NO: 468) (with underlying restriction sites BamHI and Kpn21 in the coding DNA to facilitate cloning). The ColE7 (SEQ ID NO: 140) catalytic domain was subcloned into the pCLS9009 backbone by restriction and ligation using Kpn2I and EagI restriction sites, yielding pCLS7865-cT11_ColE7 (pCLS9939, SEQ ID NO: 231, encoding the protein of SEQ ID NO: 435). The fusion contains the dipeptide -GSSG- (SEQ ID NO: 468) linking the TALE-derived DNA binding domain and ColE7-derived catalytic domain.

The DNA sequence coding for the RVDs to target the AvrBs3 site (SEQ ID NO: 152) was subcloned into plasmid pCLS9939 (SEQ ID NO: 231) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TALE-AvrBs3::ColE7 construct cT11Avr_ColE7 (pCLS9940, SEQ ID NO: 232, encoding the protein of SEQ ID NO: 436). The TALE-AvrBs3::ColE7 construct was sequenced and the insert transferred to additional vectors as needed (see below).

The final TALE-AvrBs3::ColE7 yeast expression plasmid, pCLS8589 (SEQ ID NO: 233), was prepared by yeast in vivo cloning using plasmid pCLS9940 (SEQ ID NO: 232). To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of plasmid (pCLS9940) linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform the yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::ColE7 construct was tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224, Table 7FIG. 22). TALE-AvrBs3::ColE7 activity levels on the respective targets in yeast cells are shown in FIG. 12.

Activity of TALE::ColE7 in Plants

The DNA sequence coding for the RVDs to target the NptIIT5-L and NptIIT6-L sites (SEQ ID NO: 276 to 279) were subcloned into plasmid pCLS15785 (SEQ ID NO: 285, a C-terminally modified ColE7 K497A mutant of plasmid pCLS9939, SEQ ID NO: 231) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequences to create the subsequent TALE::ColE7_A497 constructs cT11NptIIT5-L_ColE7_A497 (pCLS15786, SEQ ID NO: 286) and cT11NptIIT6-L_ColE7_A497 (pCLS15787, SEQ ID NO: 287), respectively. The constructs were sequenced and the TALE::ColE7_A497 inserts transferred by standard cloning techniques to plasmid pCLS14529 (SEQ ID NO: 282) to generate the final TALE-NptIIT5-L::ColE7_A497 and TALE-NptIIT6-L::ColE7_A497 expression plasmids, pCLS14584 (SEQ ID NO: 288, encoding the protein of SEQ ID NO: 437) and pCLS14587 (SEQ ID NO: 289, encoding the protein of SEQ ID NO: 438), respectively. Plasmid pCLS14529 allows for cloning gene of interest sequences downstream of a promoter that confers high levels of constitutive expression in plant cells.

To test activity in plant cells, a YFP-based single-strand annealing (SSA) assay was employed. The YFP reporter gene has a short duplication of coding sequence that is interrupted by either an NptIIT5 or NptIIT6 TALEN target site. Cleavage at the target site stimulates recombination between the repeats, resulting in reconstitution of a functional YFP gene. To quantify cleavage, the reporter is introduced along with a construct encoding a FokI-based TALEN or compact TALEN into tobacco protoplasts by PEG-mediated transformation. Uniform transformation efficiencies were obtained by using the same amount of plasmid in each transformation—i.e. 15 μg each of plasmids encoding YFP and either the TALEN or cTALEN. After 24 hours, the protoplasts were subjected to flow cytometry to quantify the number of YFP positive cells. The TALE:: ColE7_A497 activity levels, using cTALENs according to the present invention, in plants were comparable to those of a FokI-based TALEN control constructs on the targets tested (Table 10).

TABLE 10 Activity of TALE-NptIIT5-L::ColE7_A497 and TALE-NptIIT6- L::ColE7_A497 on appropriate DNA targets. TALEN Construct TALE- TALE- Target NptIIT5-L:: NptII5.1 NptIIT6-L:: NptII6.1 DNA ColE7_A497 control ColE7_A497 control NptII5.1 + + n.a. n.a. NptII6.1 n.a. n.a. + + Relative activity is scaled to the control constructs as: n.a., not applicable; +, 100% activity of control (8% YFP positive cells).

Engineering of the TALE::ColE7

Variants differing by truncations of the C-terminal domain of the AvrBs3-derived TALEN (SEQ ID NO: 196) are chosen as starting scaffolds. A subset of these variants includes truncation after positions E886 (C0), P897 (C11), G914 (C28), L926 (C40), D950 (C64), R1000 (C115), D1059 (C172) (the protein domains of truncated C-terminal domains C11 to C172 are respectively given in SEQ ID NO: 204 to 209) and P1117 [also referred as Cter wt or WT Cter (SEQ ID NO: 210) lacking the activation domain of the C-terminal domain of natural AvrBs3 (SEQ ID NO: 220)]. The plasmids coding for the variant scaffolds containing the AvrBs3-derived N-terminal domain, the AvrBs3-derived set of repeat domains and the truncated AvrBs3-derived C-terminal domain [pCLS7821, pCLS7803, pCLS7807, pCLS7809, pCLS7811, pCLS7813, pCLS7817 (SEQ ID NO: 211 to 217) which are based on the pCLS7184 (SEQ ID NO: 196)] allow cloning of any catalytic domain in fusion to the C-terminal domain, using the restriction sites BamHI and EagI.

The DNA corresponding to the catalytic domain of ColE7 is amplified by the PCR to introduce, at the DNA level, a BamHI (at the 5′ of the coding strand) and a EagI (at the 3′ of the coding strand) restriction site and, at the protein level, a linker (for example -SGGSGS- stretch, SEQ ID NO: 219) between the C terminal domain of the TALE and the ColE7 catalytic domain. Additionally, variants of the ColE7 endonuclease domain that modulate catalytic activity can be generated having changes (individually or combined) at the following positions: K446, R447, D493, R496, K497, H545, N560 and H573 [positions refer to the amino acid sequence of the entire ColE7 protein (SEQ ID NO: 11)]. The final TALE::ColE7 constructs are generated by insertion of the ColE7 catalytic domain into the scaffold variants using BamHIH and EagI and standard molecular biology procedures.

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::ColE7 constructs are tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::Fold TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224, Table 7FIG. 22).

Example 3e TALE::CreI Compact TALEN

The wild-type I-CreI meganuclease (SEQ ID NO: 106) was chosen as a protein template to derive a sequence-specific catalytic domain that when fused to a TALE-derived scaffold (composed of a N-terminal domain, a central core composed of RVDs and a C-terminal domain) would generate a new class of cTALEN (TALE::CreI). To distinguish the orientation (N-terminal vs. C-terminal) of the catalytic domain (CD) fusions, construct names are written as either CD::TALE-RVD (catalytic domain is fused N-terminal to the TALE domain) or TALE-RVD::CD (catalytic domain is fused C-terminal to the TALE domain), where “-RVD” optionally designates the sequence recognized by the TALE domain and “CD” is the catalytic domain type. Herein, we describe novel TALE::CreI-based constructions that target for example the T cell receptor B gene (TCRB gene, SEQ ID NO: 290, FIG. 13) sequence, both via the TALE DNA binding domain and the re-engineered I-CreI domain. Notably, specificity of the TALE::CreI compact TALEN is driven by both the TALE DNA binding domain as well as the I-CreI-derived catalytic domain. In a compact TALEN context, such proteins can provide, within a reasonably-sized monomeric protein, the requisite high specificity demanded by therapeutic applications.

Activity of TALE::CreI in Yeast

A core TALE scaffold, sT2 (SEQ ID NO: 135), was selected onto which (a) different sets of RVD domains could be inserted to change DNA binding specificity, and; (b) a selection of I-CreI-derived catalytic domains could be attached, N- or C-terminal, to effect DNA cleavage (or nicking). As previously mentioned, the sT2 truncated scaffold was generated by the PCR from a full-length core TALEN scaffold template (pCLS7183, SEQ ID NO: 141) using primers CMP_G061 (SEQ ID NO: 142) and CMP_G065 (SEQ ID NO: 143) and was cloned into vector pCLS7865 (SEQ ID NO: 144) to generate pCLS7865-cTAL11_CFS1 (pCLS9009, SEQ ID NO: 145), where CFS1 designates the amino acid sequence -GSSG- (SEQ ID NO: 468) (with underlying restriction sites BamHI and Kpn21 in the coding DNA to facilitate cloning). A re-engineered I-CreI catalytic domain, designed to target a sequence in the T cell receptor B gene (TCRB gene, SEQ ID NO: 290, FIG. 13), was subcloned in two steps. First, the I-CreI_NFS1 (SEQ ID NO: 122) scaffold, where NFS1 (SEQ ID NO: 98) comprises a linker of 20 amino acids -GSDITKSKISEKMKGQGPSG- (SEQ ID NO: 98) (with underlying restriction sites BamHI and Kpn21 in the coding DNA to facilitate cloning), was fused to the pCLS7865-cTAL11_CFS1 scaffold (using BamHIH and EagI restriction sites) to insert the NFS1 linker in-frame to the coding sequence. The I-CreI meganuclease was subsequently replaced by the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291) construct using Kpn2I and XhoI restriction sites, yielding pCLS7865-cT11_scTB2aD01 (pCLS15788, SEQ ID NO: 292, encoding the protein of SEQ ID NO: 439). Two point-mutant variants of the TCRB02-A meganuclease, TCRB02-A_148C (pCLS12083, SEQ ID NO: 293, encoding the protein of SEQ ID NO: 442) and TCRB02-A_333C (pCLS12195, SEQ ID NO: 294, encoding the protein of SEQ ID NO: 443), were also subcloned as catalytic domains fused to a TALE binding core, yielding constructs pCLS7865-cT11_scTB2aD01_148C (pCLS15789, SEQ ID NO: 295, encoding the protein of SEQ ID NO: 440) and pCLS7865-cT11_scTB2aD01_333C (pCLS15790, SEQ ID NO: 296, encoding the protein of SEQ ID NO: 441).

Three DNA sequences coding for RVDs that target the TCRB gene were designed at different distances from the meganuclease site, leading to RVDs TCRBO2A1 (SEQ ID NO: 297), TCRB02A2 (SEQ ID NO: 298) and TCRBO2A3 (SEQ ID NO: 299) that target sequences located 7 bp, 12 bp and 16 bp, respectively, upstream of the meganuclease TCRB site (FIG. 13). DNA sequences for each RVD were independently subcloned into plasmid pCLS15788 (SEQ ID NO: 292) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TALE::scTB2aD01 constructs cT11TB2A1_scTB2aD01 (pCLS15791, SEQ ID NO: 300), cT11TB2A2_scTB2aD01 (pCLS15792, SEQ ID NO: 301) and cT11TB2A3_scTB2aD01 (pCLS15793, SEQ ID NO: 302). Additionally, the TCRBO2A2 (SEQ ID NO: 298) RVDs were similarly cloned into pCLS15789 (SEQ ID NO: 295) to create cT11TB2A2_scTB2aD01_148C (pCLS15794, SEQ ID NO: 303). All constructs were sequenced and the various inserts transferred to additional vectors as needed (see below).

The final TALE::scTB2aD01 yeast expression plasmids, pCLS13449 (SEQ ID NO: 304, encoding the protein of SEQ ID NO: 444), pCLS13450 (SEQ ID NO: 305, encoding the protein of SEQ ID NO: 445), pCLS13451 (SEQ ID NO: 306, encoding the protein of SEQ ID NO: 446) and pCLS15148 (SEQ ID NO: 307, encoding the protein of SEQ ID NO: 455), were prepared by yeast in vivo cloning using plasmids pCLS15791 (SEQ ID NO: 300), pCLS15792 (SEQ ID NO: 301), pCLS15793 (SEQ ID NO: 302) and pCLS15794 (SEQ ID NO: 303), respectively. To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of each plasmid linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform, respectively, the yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN or meganuclease DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE::scTB2aD01-based constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on hybrid targets TCRBO2Tsp7 (SEQ ID NO: AC4), TCRBO2Tsp12 (SEQ ID NO: AC5) and TCRBO2Tsp16 (SEQ ID NO: AC6), illustrated in FIG. 14. The TCRB02.1-only target was included to compare activity with the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291), which does not require the TALE DNA binding sites for activity. Activity levels on the respective targets in yeast cells for the indicated TALE::scTB2aD01-based constructs are shown in FIG. 14. Notably, under the in vivo conditions tested the TALE-TB2A2::scTB2aD01_148C (pCLS15794, SEQ ID NO: 303) construct no longer cleaves targets lacking the DNA sequence recognized by the TALE DNA binding moiety.

Activity of TALE::CreI in Mammalian Cells

DNA encoding the TALE-TB2A2::scTB2aD01 and TALE-TB2A3::scTB2aD01 constructs from pCLS15792 (SEQ ID NO: 301) and pCLS15793 (SEQ ID NO: 302) were subcloned into the pCLS1853 (SEQ ID NO: 193) mammalian expression plasmid using Ascl and XhoI restriction enzymes for the receiving plasmid and BssHII and XhoI restriction enzymes for TALE::scTB2aD01-based inserts, leading to the mammalian expression plasmids pCLS14894 and pCLS14895 (SEQ ID NO: 308 and 309), respectively.

All mammalian target reporter plasmids containing the TALEN DNA target sequences were constructed using the standard Gateway protocol (INVITROGEN) into a CHO reporter vector (Arnould, Chames et al. 2006, Grizot, Epinat et al. 2010).

To monitor protein expression levels, TALE::scTB2aD01-based constructs were transfected in mammalian cells (HEK293) alongside the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291). Briefly, cells were transfected, respectively, with 300 ng of each protein encoding plasmid in the presence of lipofectamine. Fourty-eight hours post-transfection, 20 μg of total protein extract for each sample was analyzed by Western-Blot using a polyclonal anti-1-CreI antibody. A typical western-blot is shown in FIG. 15.

Relative toxicity of the TALE::scTB2aD01-based constructs was assessed using a cell survival assay. CHOK1 cells were used to seed plates at a density of 2.5*10³ cells per well. The following day, varying amounts of plasmid encoding either the TALE::scTB2aD01-based constructs (pCLS14894 and pCLS14895; SEQ ID NO: 308 and 309) or the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291) and a constant amount of GFP-encoding plasmid (10 ng) were used to transfect the cells with a total quantity of 200 ng using Polyfect reagent. GFP levels were monitored by flow cytometry (Guava Easycyte, Guava technologies) on days 1 and 6 post-transfection. Cell survival is expressed as a percentage, calculated as a ratio (TALEN and meganuclease-transfected cells expressing GFP on Day 6/control-transfected cells expressing GFP on Day 6) corrected for the transfection efficiency determined on Day 1. Typical cell survival assay data are shown in FIG. 16.

Cleavage activity in vivo was monitored via detection of NHEJ events in the presence of TREX2 exonuclease. Plasmid (3 μg) encoding either the TALE::scTB2aD01-based constructs (pCLS14894 and pCLS14895; SEQ ID NO: 308 and 309) or the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291) and 2 μg of scTrex2-encoding plasmid (pCLS8982, SEQ ID NO: 310) were used to transfect the HEK293 cells in the presence of lipofectamine. Genomic DNA was extracted 2 and 7 days post-transfection with the DNeasy Blood and Tissue kit (Qiagen) and the region encompassing the TCRB02 site (FIG. 13) was amplified using the PCR with oligos TRBC2F3 (Seq ID NO: 311) and TRBC2R3B (SEQ ID NO: 312) at day 2 post-transfection and with oligos TRBC2F4 (SEQ ID NO: 315) and TRBC2R4B (SEQ ID NO: 314) at day 7 post-transfection. Respective PCR products (100 ng) were heat denatured, allowed to re-anneal by slow-cooling then treated with T7 endonuclease 1 (NEB) for 15 minutes at 37° C. Digested PCR products are separated on 10% acrylamide gels and visualized with SYBRgreen (Invitrogen) staining. Cleavage of mismatched DNA sequences by T7 endonuclease is indicative of NHEJ events resulting from the activity of the cTALEN or meganuclease at the targeted locus. FIG. 17 illustrates the detectable NHEJ activity of the TALE::scTB2aD01-based constructs (pCLS14894 and pCLS14895; SEQ ID NO: 308 and 309) compared to the engineered TCRB02-A meganuclease (pCLS6857, SEQ ID NO: 291). Whereas at day 2 NHEJ results are comparable for all constructs, NHEJ activity at day 7 can only be detected for the TALE::scTB2aD01-based constructs, suggesting that these compact TALENs do not induce cytotoxicity.

Engineering of the TALE::CreI

A significant novel property of the TALE::CreI compact TALEN resides in the ability to independently engineer the “hybrid” specificity of the final molecule. As such, the inherent activity/specificity ratio can be modulated within the TALE::CreI-derived constructs, allowing for unprecedented specific targeting with retention of high DNA cleavage activity. In its simplest form, successful re-targeting of the TALE DNA binding domain is achieved via the RVD cipher (FIG. 3), with a pseudo one-to-one correspondence to the underlying DNA base. Engineering of the I-CreI moiety, however, presents more challenges insomuch as there exists a potential codependence of protein-DNA contacts needed for suitable DNA binding and cleavage activity. Methods have been described (WO2006097854, WO2008093249, WO03078619, WO2009095793, WO 2007/049095, WO 2007/057781, WO 2006/097784, WO 2006/097853, WO 2007/060495, WO 2007/049156 and WO 2004/067736) to successfully re-engineer the I-CreI meganuclease to target novel DNA sequences. As some of these methods rely on a clustered approach, it can be envisioned that using said approach the “absolute” specificity of the I-CreI moiety could be reduced in a stepwise manner. For example, the breakdown of the I-CreI DNA interaction surface into discrete 10NNN, 7NN, 5NNN and 2NN regions (per monomeric subunit half) allows for novel engineering wherein high specificity is maintained in the central 5NNN-2NN region at the expense of “loose” or broad specificity in the outer 10NNN-7NN regions. In essence such an approach could reduce the complexity of re-engineering the I-CreI-derived scaffold for a compact TALEN context as only “selectivity” in cleavage is required for the catalytic domain, with subsequent specificity provided by the TALE DNA binding part of the protein fusion. Taken together, the ease of engineering combined with the potential high specificity and high DNA cleavage activity make TALE::CreI-derived compact TALENs ideal tools for therapeutic applications. Finally, it should be noted that the I-CreI moiety could in principle be replaced with a host of naturally existing or re-engineered homing endonuclease-derived catalytic domains.

Example 3f Activity of TALE::SnaseSTAUU

Activity of TALE::SnaseSTAUU in Yeast

Variants differing by truncations of the C-terminal domain of the AvrBs3-derived TALEN (SEQ ID Na: 196) are chosen as starting scaffolds. A subset of these variants includes truncation after positions G914 (C28) and L926 (C40) (the protein domains of truncated C-terminal domains C28 and C40 are respectively given in SEQ ID NO: 205 and 206). The plasmids coding for the variant scaffolds containing the AvrBs3-derived N-terminal domain, the AvrBs3-derived set of repeat domains and the truncated AvrBs3-derived C-terminal domain [pCLS7807 and pCLS7809, (SEQ ID NO: 213 and 214) which are based on the pCLS7184 (SEQ ID Na: 196)] allow cloning of any catalytic domain in fusion to the C-terminal domain, using the restriction sites BamHI and EagI.

The DNA corresponding to amino acid residues 83 to 231 of SnaseSTAAU (SEQ ID NO: 30) is amplified by the PCR to introduce, at the DNA level, a BamHI (at the 5′ of the coding strand) and a EagI (at the 3′ of the coding strand) restriction site and, at the protein level, a linker (for example -SGGSGS- stretch, SEQ ID NO: 219) between the C terminal domain of the TALE and the SnaseSTAAU catalytic domain. The final TALE::SnaseSTAAU constructs are generated by insertion of the SnaseSTAAU catalytic domain into the scaffold variants using BamHI and EagI and standard molecular biology procedures. Scaffold variants truncated after positions G914 (C28) and L926 (C40), respectively encoded by pCLS7807 and pCLS7809, (SEQ ID NO: 213 and 214), were fused to the SnaseSTAAU catalytic domain (SEQ ID NO: 30), leading to pCLS9082 and pCLS9081 (SEQ ID NO: 370 and 371). The cloning step also brings at the amino acid level an AAD sequence at the Cter of the SnaseSTAAU catalytic domain.

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-AvrBs3::SnaseSTAAU constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN, which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, TALE-AvrBs3::SnaseSTAAU constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224). Data summarized in FIG. 19 show that TALE-AvrBs3::SnaseSTAAU constructs are active on targets having two AvrBs3 recognition site, according to the chimeric protein of the present invention, but also on targets containing only one AvrBs3 recognition site.

Example 4

Basic cTALENs are composed of a single DNA binding domain fused to a single catalytic domain and are designed to stimulate HR via a single double-strand DNA cleavage or single-strand nicking event. For certain applications (e.g. gene inactivation), it is favorable to enhance the level of NHEJ. This example illustrates the creation of a dual-cleavage cTALEN (dcTALEN) that is capable of effecting cleavage of double-strand DNA at two distinct sites flanking the TALE DNA binding domain (FIG. 5C). The simultaneous cleavage of the DNA at the two sites is expected to eliminate the intervening sequence and therefore abolish “scarless” re-ligation by NHEJ (FIG. 1).

The baseline scaffolds (SEQ ID NO: 136 to SEQ ID NO: 139) described in Example 3 are used as starting points for fusion designs. A non-exhaustive list of catalytic domains amenable to fusion with TALE DNA binding domains is presented in Table 2. A non-exhaustive list of linkers that can be used is presented in Table 3. See examples 3, 5, 6 and 7 for additional details concerning the choice of linker or enhancement domain. For the dcTALEN designs, at least one cleavase domain is fused (N- or C-terminal) to the TALE DNA binding domain. The additional catalytic domain can be either a nickase of cleavase (endonuclease or exonuclease) domain, and depends on the nature of the application. For example, the coupling of a cleavase domain on one side with a nickase domain on the other could result in excision of a single-strand of DNA spanning the TALE DNA binding region. The targeted generation of extended single-strand overhangs could be applied in applications that target DNA repair mechanisms. For targeted gene inactivation, the use of two cleavase domains in the dcTALEN is preferred.

All dcTALEN designs are assessed using our yeast assay (see Example 1) and provide detectable activity comparable to existing engineered meganucleases. Furthermore, potential enhancements in NHEJ are monitored using the mammalian cell based assay as described in Example 3.

Example 4a Activity of TevI::TALE::FokI and TevI::TALE::TevI Dual Cleavage TALENs

Dual cleavage TALENs (CD::TALE::CD), possessing an N-terminal I-TevI-derived catalytic domain and a C-terminal catalytic domain derived from either FokI (SEQ ID NO:368) or I-TevI (SEQ ID NO: 20), were generated on the baseline bT2-Avr (SEQ ID NO: 137) scaffold. The catalytic domain fragment of I-TevI was excised from plasmid pCLS12731 (SEQ ID NO: 236) and subcloned into vectors pCLS15795 (SEQ ID NO: 351) and pCLS9013 (SEQ ID NO: 153) by restriction and ligation using NcoI and NsiI restriction sites, yielding TevD02_cT11Avr_FokI-L (pCLS15796, SEQ ID NO: 352, encoding the protein of SEQ ID NO: 447) and TevD02_cT11Avr_TevD02 (pCLS15797, SEQ ID NO: 353, encoding the protein of SEQ ID NO: 448), respectively. All constructs were sequenced and the insert transferred to additional vectors as needed (see below).

The final TevI::TALE-AvrBs3::FokI and TevI::TALE-AvrBs3::TevI yeast expression plasmids, pCLS13299 (SEQ ID NO: 354, encoding the protein of SEQ ID NO: 449) and pCLS13301 (SEQ ID NO: 355, encoding the protein of SEQ ID NO: 450), were prepared by yeast in vivo cloning using plasmids pCLS15796 (SEQ ID NO: 352) and pCLS15797 (SEQ ID NO: 353), respectively. To generate an intact coding sequence by in vivo homologous recombination, approximately 40 ng of each plasmid linearized by digestion with BssHII and 1 ng of the pCLS0542 (SEQ ID NO: 156) plasmid DNA linearized by digestion with NcoI and EagI were used to transform, respectively, the yeast S. cerevisiae strain FYC2-6A (MATa, trp1Δ63, leu2Δ1, his3Δ200) using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TevI::TALE-AvrBs3::FokI and TevI::TALE-AvrBs3::TevI constructs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21). In addition, constructs were tested on a target having only a single AvrBs3 or RagT2-R recognition site (SEQ ID NO: 238, Table 11). On suitable targets, the TevI::TALE-AvrBs3::FokI and TevI::TALE-AvrBs3::TevI activity levels in yeast were comparable to those of their parent molecules lacking the N-terminal I-TevI-derived catalytic domain. Significant activity is illustrated in table 11 for a sample single-site target, according to the dcTALEN of the present invention.

TABLE 11 Activity of various cTALENs and dcTALENs on dual- and single-site DNA targets. Target DNA Avr25RAGT2R Avr25 (dual-site) (single-site) TALEN Construct (SEQ ID NO: 177) (SEQ ID NO: 238) TevI::TALE-AvrBs3 ++++ +++ TALE-AvrBs3::FokI ++++ n.d. TALE-AvrBs3::TevI ++++ n.d. TevI::TALE-AvrBs3::FokI ++++ +++ TevI::TALE-AvrBs3::TevI ++++ +++ Relative activity is scaled as: n.d., no activity detectable; +, <25% activity; ++, 25% to <50% activity; +++, 50% to <75% activity; ++++, 75% to 100% activity.

Example 4b scTrex2::TALE::FokI Dual Cleavage TALEN

A dual cleavage TALEN(CD::TALE::CD), possessing an N-terminal scTrex2-derived catalytic domain and a C-terminal catalytic domain derived from FokI, was generated on the baseline bT2-Avr (SEQ ID NO: 137) scaffold. The catalytic domain fragment of scTrex2 was excised from plasmid pCLS15798 (SEQ ID NO: 356, encoding the protein of SEQ ID NO: 451) and subcloned into vector pCLS15795 (SEQ ID NO: 351) by restriction and ligation using NcoI and NsiI restriction sites, yielding scTrex2_cT11Avr_FokI-L (pCLS15799, SEQ ID NO: 357, encoding the protein of SEQ ID NO: 452). The construct was sequenced and the insert transferred to additional vectors as needed (see below).

DNA encoding the TALE-AvrBs3::FokI or scTrex2::TALE-AvrBs3::FokI constructs from either pCLS15795 (SEQ ID NO: 351) or pCLS15799 (SEQ ID NO: 357), respectively, was subcloned into the pCLS1853 (SEQ ID NO: 193) mammalian expression plasmid using Ascl and XhoI restriction enzymes for the receiving plasmid and BssHII and XhoI restriction enzymes for the inserts, leading to the mammalian expression plasmids pCLS14972 and pCLS14971 (SEQ ID NO: 358 and 359), respectively.

All mammalian target reporter plasmids containing the TALEN DNA target sequences were constructed using the standard Gateway protocol (INVITROGEN) into a CHO reporter vector (Arnould, Chames et al. 2006, Grizot, Epinat et al. 2010). The TALE-AvrBs3::FokI and scTrex2::TALE-AvrBs3::FokI constructs were tested in an extrachromosomal assay in mammalian cells (CHO K1) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN, which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 21).

For this assay, CHO K1 cells were transfected in a 96-well plate format with 75 ng of target vector and an increasing quantity of each variant DNA from 0.7 to 25 ng, in the presence of PolyFect reagent (1 μL per well). The total amount of transfected DNA was completed to 125 ng (target DNA, variant DNA, carrier DNA) using an empty vector. Seventy-two hours after transfection, culture medium was removed and 150 μl of lysis/revelation buffer for β-galactosidase liquid assay was added. After incubation at 37° C., optical density was measured at 420 nm. The entire process is performed on an automated Velocityll BioCel platform (Grizot, Epinat et al. 2009).

Activity levels in mammalian cells on suitable targets for the scTrex2::TALE-AvrBs3::FokI construct were comparable to those of the parent TALE-AvrBs3::FokI molecule, indicating that the extra scTrex2 moiety does not impair the TALEN DNA cleavage function. Assessment of the scTrex2 function is performed in assays suitable for the detection of NHEJ events.

Example 5

Baseline designs for the cTALEN scaffolds are based on established TALE DNA binding domains. Compact TALENs are designed to be as small and efficient as possible. To obtain this goal it may therefore be necessary to enlist “enhancer” domains to bridge the functional gap between compact TALE DNA binding domains and the various catalytic domains. FIGS. 6 (A-E) illustrates various non-exhaustive configurations wherein such enhancer domains can be applied. Note that the figure is illustrative only, and N- vs. C-terminal variations are implied (i.e. FIG. 6A can also have an N-terminal enhancer domain and C-terminal catalytic domain). Tables 1 and 2 lists potential enhancer domains that could assist in DNA binding (specific and non-specific contacts).

Enhanced TALENs (eTALENs) are created using functional cTALENS from Example 3. The addition of the enhancer domain is evaluated in our yeast assay (see Example 1). A particular enhancer domain is judged useful if it provides a minimal 5% enhancement in efficiency of the starting cTALEN, more preferably a minimal 10% enhancement, more preferably 20%, more preferably 30%, more preferably 40%, more preferably 50%, again more preferably an enhancement greater than 50%.

Example 5a TALE::ColE7::TALE Enhanced TALENs

Enhanced TALENs (TALE::CD::TALE), possessing N- and C-terminal TALE DNA binding domains bordering a central DNA cleavage domain, were generated using the sT2 (SEQ ID NO: 135) core scaffold. The layout of this class of compact TALEN is illustrated in FIG. 6B, wherein the N-terminal “enhancer domain” is itself a TALE DNA binding domain. A point-mutant derivative of the ColE7 catalytic domain (pCLS15785, SEQ ID NO: 285) was chosen for the catalytic core of the eTALEN. Two final constructs, TALE-AvrBs3::ColE7_A497::TALE-RagT2-R (pCLS15800, SEQ ID NO: 360, encoding the protein of SEQ ID NO: 453) and TALE-RagT2-R::ColE7_A497::TALE-AvrBs3 (pCLS15801, SEQ ID NO: 361, encoding the protein of SEQ ID NO: 454), were obtained using standard molecular cloning techniques with DNA sequences from sT2 (SEQ ID NO: 135), pCLS15785 (SEQ ID NO: 285), AvrBs3 (SEQ ID NO: 152) and RagT2-R (SEQ ID NO: 271) as templates. All TALE::CD::TALE constructs were sequenced and the inserts transferred to additional vectors as needed (see below).

The final TALE::CD::TALE-based yeast expression plasmids, pCLS12106 (SEQ ID NO: 362) and pCLS12110 (SEQ ID NO: 363, were prepared by restriction and ligation using NcoI and EagI restriction sites to subclone into the pCLS0542 (SEQ ID NO: 156) plasmid. The yeast S. cerevisiae strain FYC2-6A (MATα, trp1Δ63, leu2Δ1, his3Δ200) was transformed using a high efficiency LiAc transformation protocol (Arnould et al. 2007).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE::CD::TALE constructs are tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on asymmetric AvrBs3/RagT2-R hybrid targets in order to compare activity with a parent compact TALEN (e.g. pCLS8589, SEQ ID NO: 233), which has activity on targets with a single binding site. In addition, constructs are tested on a target having only a single AvrBs3 or RagT2-R recognition site.

Example 6

To date, all known TAL effectors and derivatives thereof appear to require a T base at positions −1 (FIG. 3) in the recognition sequence. To overcome this limitation, an enhancer domain is used to replace the N-terminal region of the TALE protein. Sequence and structure-based homology modeling of the N-terminal TALE region of bT2-derivatives have yielded three potential candidate proteins (Table 1): (i) Fem-3 binding factor, SEQ ID NO: 4, (FBF1, Puf family of RNA binding proteins) from C. elegans; (ii) artificial alpha-helicoidal repeat proteins (aRep), SEQ ID NO: 5 and; (iii) proteins of the Ankyrin super-family. The content and arrangement of secondary structure elements allows for using these models as starting points for enhancer domains that replace the N-terminal region of the TALE protein.

Chimeric proteins are constructed using the analogous regions from one of the 3 candidates mentioned to replace the N-terminal TALE protein region up to the first canonical repeat domain. The new interface is redesigned in silico, using the homology models as guides. This approach can be used to pinpoint the determinants of specificity for the requisite T at position −1 of the target sequence. The replacement enhancer domain should at minimum provide structural integrity to the cTALEN protein. Constructs are evaluated in our yeast assay (see Example 1). A particular enhancer domain is judged useful if it provides a minimal 5% retention in activity of the starting cTALEN in the absence of a T at target position −1, more preferably a minimal 10% retention, more preferably 20%, more preferably 30%, more preferably 40%, more preferably 50%, again more preferably a retention in activity greater than 50%.

Example 7

To generate more suitable and compact scaffolds for cTALENS, the nature of the C-terminal region (beyond the final half-repeat domain) of the TALE protein has been analyzed. Sequence and structure-based homology modeling of the C-terminal TALE region of bT2-derivatives have yielded three potential candidate proteins (Table 1): (i) the hydrolase/transferase of Pseudomonas Aeuriginosa, SEQ ID NO: 6; (ii) the Polymerase domain from the Mycobacterium tuberculosis Ligase D, SEQ ID NO: 7; (iii) initiation factor eIF2 from Pyrococcus, SEQ ID NO: 8; (iv) Translation Initiation Factor Aif2betagamma, SEQ ID NO: 9. As in example 6, homology models are used to pinpoint regions for generating possible C-terminal truncations; potential truncation positions include 28, 40, 64, 118, 136, 169, 190 residues remaining beyond the last half-repeat domain. Additionally, homologous regions from the aforementioned proteins can be used to replace the C-terminal domain entirely. Contact prediction programs can be used to identify, starting from the primary sequence of a protein, the pairs of residues that are likely proximal in the 3D space. Such chimeric proteins should provide more stable scaffolds on which to build cTALENs.

Constructs are evaluated in our yeast assay (see Example 1). A particular enhancer domain is judged useful if it provides a minimal 5% retention in activity of the starting cTALEN, more preferably a minimal 10% retention, more preferably 20%, more preferably 30%, more preferably 40%, more preferably 50%, again more preferably a retention in activity greater than 50%.

Example 8

To generate compact TALENS with alternative activities, trans cTALENS are generated by (a) using a catalytic domain with separable activities (FIG. 7A, B), or; (b) providing an auxiliary activity as a TALE-fusion (FIG. 7C). Sequence and structure-based modeling of class III (Chan, Stoddard et al. 2011). TypellS restriction endonucleases (REases) were used to create trans TALENs (see Table 2 for a non-exhaustive list). The initial trans TALEN is generated via fusion of an independently active catalytic domain (e.g. the Nt.BspD6I nickase) as described in Examples 3 and 4. In principle this trans TALEN can be used as is depending on the application. To convert the cTALEN to a functional trans TALEN, the auxiliary domain (in this case, ss.BspD6I) is provided in trans (FIG. 8A). Such optionally trans and/or heterodimeric proteins can allow for cTALEN scaffolds with activity that can be modulated to a given application.

Constructs are evaluated in our yeast assay (see Example 1). A particular auxiliary domain is judged useful if it provides an alternative activity to that of the starting cTALEN.

If the auxiliary domain used exhibits activity independent of the initial cTALEN (i.e. in a non-trans TALEN context), it can as well be fused to a TALE domain for specific targeting (FIG. 7B). Auxiliary domains can also be provided in trans as targeted entities to provide functions unrelated to the cTALEN (FIG. 7C).

Example 8a Specific Inhibition of TALEN Catalytic Activity

As mentioned in examples 3c and 3d, both NucA (SEQ ID NO: 26) and ColE7 (SEQ ID NO: 140) can be inhibited by complex formation with their respective inhibitor proteins, NuiA (SEQ ID NO: 229) and Im7 (SEQ ID NO: 230). Colicin-E9 (SEQ ID NO: 366) is another non-limiting example of protein which can be inhibited by its respective inhibitor Im9 (SEQ ID NO: 369). With respect to TALENs derived from the NucA (TALE::NucA) or ColE7 (TALE::ColE7) catalytic domains, the inhibitors serve as auxiliary domains (FIG. 7A) that modulate the activity by preventing DNA cleavage.

The Im7 (SEQ ID NO: 230) and NuiA (SEQ ID NO: 229) inhibitor proteins were subcloned into the pCLS7763 backbone (SEQ ID NO: 241) by restriction and ligation using NcoI and EagI restriction sites, yielding pCLS9922 (SEQ ID NO: 242) and pCLS9923 (SEQ ID NO: 243), respectively. These plasmids were then used in co-transformation experiments in the standard yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

TALE-AvrBs3::NucA (pCLS9924, SEQ ID NO: 223) and TALE-AvrBs3::ColE7 (pCLS8589, SEQ ID NO: 233) constructs were tested in a yeast SSA assay on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN (pCLS8590, SEQ ID NO: 244), which requires two binding sites for activity. AvrBS3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: 157 to 192, FIG. 22). In addition, constructs were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224, FIG. 22). Activity modulation of the TALENs was assessed in the presence or absence of specific or unspecific inhibitor protein, using the TALE-AvrBs3::FokI TALEN as control.

Data summarized in table 12 indicate that TALE-AvrBs3::NucA and TALE-AvrBs3::ColE7 constructs are specifically inactivated by the presence of their respective inhibitor proteins NuiA and Im7, according to the present invention.

TABLE 12 Activity of TALEN constructs in the presence of inhibitor protein. Inhibitor Protein TALEN Construct None NuiA Im7 TALE-AvrBs3::NucA (SEQ ID NO: 223) ++++ n.d. ++++ TALE-AvrBs3::ColE7 (SEQ ID NO: 233) ++++ ++++ n.d. TALE-AvrBs3::FokI (SEQ ID NO: 244) ++++ ++++ ++++ Relative activity is scaled as: n.d., no activity detectable; +, <25% activity; ++, 25% to <50% activity; +++, 50% to <75% activity; ++++, 75% to 100% activity.

Example 8b Enhancing TALEN Catalytic Activity Via a Trans TALEN

Example 3b illustrates that the TevI::TALE functions unassisted as a compact TALEN (pCLS8522, SEQ ID NO: 237). To further enhance activity, a trans TALEN was designed using a TALE::TevI construct in a layout depicted in FIG. 7C. The DNA sequence coding for the RVDs to target the RagT2-R site (SEQ ID NO: 271) was subcloned into plasmid pCLS7865-cT11_TevD02 (pCLS9011, SEQ ID NO: 151) using Type IIS restriction enzymes BsmBI for the receiving plasmid and BbvI and SfaNI for the inserted RVD sequence to create the subsequent TALE-RagT2-R::TevI construct cT11RagT2_R_TevD02 (pCLS15802, SEQ ID NO: 364). The construct was sequenced and the insert subcloned into the pCLS7763 backbone (SEQ ID NO: 241) by restriction and ligation using NcoI and EagI restriction sites, yielding pCLS8990 (SEQ ID NO: 365). Plasmid pairs pCLS8522 (SEQ ID NO: 237) and pCLS7763 (SEQ ID NO: 241) or pCLS8522 (SEQ ID NO: 237) and pCLS8990 (SEQ ID NO: 365) were then used in co-transformation experiments in the standard yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

All the yeast target reporter plasmids containing the TALEN DNA target sequences were constructed as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006).

The TALE-RagT2-R::TevI/TevI::TALE-AvrBs3 construct pairs were tested in a yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on asymmetric RagT2-R/AvrBs3 hybrid targets in order to compare activity with a parent compact TALEN (e.g. pCLS8522, SEQ ID NO: 237), which has activity on targets with a single binding site. RagT2-R/AvrBs3 hybrid targets contain two different recognition sequences juxtaposed with the 3′ end of the first (RagT2-R) proximal to the 5′ end of the second (AvrBs3) and separated by “spacer” DNA ranging from 5 to 40 bps (SEQ ID NO: G064 to G099, Table 13). FIG. 18 illustrates the modulation in TevI::TALE-AvrBs3 activity provided by the TALE-RagT2-R::TevI construct, according to the trans cTALEN of the present invention.

Example 9 Replacement of the C-Terminal Domain by a Polypeptide Linker, Activity with colE7 Catalytic Domain

We generated a first library of 37 different linkers. Many of them have a common structure comprising a variable region encoding 3 to 28 amino acids residues and flanked by regions encoding SGGSGS stretch (SEQ ID NO: 219) at both the 5′ and a 3′ end (SEQ ID NO: 372 to 408). These linkers contain XmaI and BamHI restriction sites in their 5′ and 3′ ends respectively. The linker library is then subcloned in pCLS7183 (SEQ ID NO: 141) via the XmaI and BamHI restriction sites to replace the C-terminal domain of the AvrBs3-derived TALEN (pCLS7184, SEQ ID NO: 196). The AvrBs3-derived set of repeat domains (RVDs) or any other RVD sequences having or lacking the terminal half RVD is cloned in this backbone library. DNA from the library is obtained, after scrapping of the colonies from the Petri dishes, using standard miniprep techniques. The FokI catalytic head is removed using BamHI and EagI restriction enzymes, the remaining backbone being purified using standard gel extraction techniques. DNA coding for ColE7 catalytic domain (SEQ ID NO: 11) was amplified by the PCR to introduce, at the DNA level, a BamHI (at the 5′ of the coding strand) and a EagI (at the 3′ of the coding strand) restriction site and, at the protein level, a linker (for example -SGGSGS- stretch, SEQ ID NO: 219) between the C terminal domain library and the catalytic head. After BamHI and EagI digestion and purification, the DNA coding for the different catalytic heads were individually subcloned into the library scaffold previously prepared.

DNA from the final library is obtained, after scrapping of the colonies from Petri dishes, using standard miniprep techniques and the resulting libraries are screened in our yeast SSA assay as previously described (International PCT Applications WO 2004/067736 and in Epinat, Arnould et al. 2003; Chames, Epinat et al. 2005; Arnould, Chames et al. 2006; Smith, Grizot et al. 2006) on pseudo palindromic targets in order to compare activity with a standard TALE-AvrBs3::FokI TALEN, which requires two binding sites for activity. AvrBs3 targets contain two identical recognition sequences juxtaposed with the 3′ ends proximal and separated by “spacer” DNA containing 15, 18, 21 and 24 bps (SEQ ID NO: 167, 170, 173 and 176, FIG. 22). In addition, constructs (SEQ ID NO: 416-419) were tested on a target having only a single AvrBs3 recognition site (SEQ ID NO: 224). Data summarized in FIG. 20 show sequences of the linker of a fraction of ColE7 constructs being active on targets having two AvrBs3 recognition sites or only one AvrBs3 recognition site.

The U.S. provisional applications to which this application claims priority as well as the corresponding PCT application being filed Apr. 5, 2012 and entitled “METHOD FOR THE GENERATION OF COMPACT TALE-NUCLEASES AND USES THEREOF” are hereby incorporated by reference in their entireties.

LIST OF CITED REFERENCES

-   Arimondo, P. B., C. J. Thomas, et al. (2006). “Exploring the     cellular activity of camptothecin-triple-helix-forming     oligonucleotide conjugates.” Mol Cell Biol 26(1): 324-33. -   Arnould, S., P. Chames, et al. (2006). Engineering of large numbers     of highly specific homing endonucleases that induce recombination on     novel DNA targets. Journal of Molecular Biology. 355: 443-58. -   Arnould, S., P. Chames, et al. (2006). “Engineering of large numbers     of highly specific homing endonucleases that induce recombination on     novel DNA targets.” J Mol Biol 355(3): 443-58. -   Arnould, S., C. Delenda, et al. (2011). “The I-CreI meganuclease and     its engineered derivatives: applications from cell modification to     gene therapy -   gzq083 [pii] 10.1093/protein/gzq083.” Protein engineering, design &     selection: PEDS 24(1-2): 27-31. -   Arnould, S., C. Perez, et al. (2007). “Engineered I-CreI derivatives     cleaving sequences from the human XPC gene can induce highly     efficient gene correction in mammalian cells.” Journal of Molecular     Biology 371(1): 49-65. -   Ashworth, J., J. J. Havranek, et al. (2006). “Computational redesign     of endonuclease DNA binding and cleavage specificity.” Nature     441(7093): 656-9. -   Bedayat, B., A. Abdolmohamadi, et al. (2010). “Sequence-specific     correction of genomic hypoxanthine-guanine phosphoribosyl     transferase mutations in lymphoblasts by small fragment homologous     replacement -   10.1089/oli.2009.0205.” Oligonucleotides 20(1): 7-16. -   Bennardo, N., A. Cheng, et al. (2008). “Alternative-NHEJ is a     mechanistically distinct pathway of mammalian chromosome break     repair.” PLoS Genet. 4(6): e1000110. -   Bennardo, N., A. Gunn, et al. (2009). “Limiting the persistence of a     chromosome break diminishes its mutagenic potential.” PLoS Genet.     5(10): e1000683. -   Boch, J., H. Scholze, et al. (2009). “Breaking the code of DNA     binding specificity of TAL-type III effectors.”Science 326(5959):     1509-12. -   Boch, J., H. Scholze, et al. (2009). “Breaking the code of DNA     binding specificity of TAL-type III effectors -   1178811 [pii] 10.1126/science.1178811.” Science 326(5959): 1509-12. -   Bolduc, J. M., P. C. Spiegel, et al. (2003). “Structural and     biochemical analyses of DNA and RNA binding by a bifunctional homing     endonuclease and group I intron splicing factor.” Genes Dev 17(23):     2875-88. -   Buis, J., Y. Wu, et al. (2008). “Mre11 nuclease activity has     essential roles in DNA repair and genomic stability distinct from     ATM activation.” Cell 135(1): 85-96. -   Capecchi, M. R. (2001). “Generating mice with targeted mutations -   10.1038/nm1001-1086 nm1001-1086 [pii].” Nature Medicine 7(10):     1086-90. -   Carroll, D. (2008). “Progress and prospects: zinc-finger nucleases     as gene therapy agents -   gt2008145 [pii] 10.1038/gt.2008.145.” Gene therapy 15(22): 1463-8. -   Chames, P., J. C. Epinat, et al. (2005). “In vivo selection of     engineered homing endonucleases using double-strand break induced     homologous recombination.” Nucleic Acids Res 33(20): e178. -   Chames, P., J. C. Epinat, et al. (2005). “In vivo selection of     engineered homing endonucleases using double-strand break induced     homologous recombination.” Nucleic Acids Research 33(20): e178. -   Chan, S. H., B. L. Stoddard, et al. (2011). “Natural and engineered     nicking endonucleases—from cleavage mechanism to engineering of     strand-specificity.” Nucleic Acids Research 39: 1-18. -   Chevalier, B., M. Turmel, et al. (2003). “Flexible DNA target site     recognition by divergent homing endonuclease isoschizomers I-CreI     and I-MsoI.” J Mol Biol 329(2): 253-69. -   Chevalier, B. S., T. Kortemme, et al. (2002). “Design, activity, and     structure of a highly specific artificial endonuclease.” Mol Cell     10(4): 895-905. -   Chevalier, B. S., R. J. Monnat, Jr., et al. (2001). “The homing     endonuclease I-CreI uses three metals, one of which is shared     between the two active sites.” Nat Struct Biol 8(4): 312-6. -   Chevalier, B. S, and B. L. Stoddard (2001). “Homing endonucleases:     structural and functional insight into the catalysts of     intron/intein mobility.” Nucleic Acids Res 29(18): 3757-74. -   Choo, Y. and A. Klug (1994). “Selection of DNA binding sites for     zinc fingers using rationally randomized DNA reveals coded     interactions.” Proceedings of the National Academy of Sciences of     the United States of America 91(23): 11168-72. -   Choo, Y. and A. Klug (1994). “Toward a code for the interactions of     zinc fingers with DNA: selection of randomized fingers displayed on     phage.” Proceedings of the National Academy of Sciences of the     United States of America 91(23): 11163-7. -   Choulika, A., A. Perrin, et al. (1995). “Induction of homologous     recombination in mammalian chromosomes by using the I-SceI system of     Saccharomyces cerevisiae.” Mol Cell Biol 15(4): 1968-73. -   Christian, M., T. Cermak, et al. (2010). “Targeting DNA     double-strand breaks with TAL effector nucleases.” Genetics 186(2):     757-61. -   Christian, M., T. Cermak, et al. (2010). “Targeting DNA     double-strand breaks with TAL effector nucleases genetics.     110.120717 [pii] 10.1534/genetics.110.120717.” Genetics 186(2):     757-61. -   Cost, G. J., Y. Freyvert, et al. (2010). “BAK and BAX deletion using     zinc-finger nucleases yields apoptosis-resistant CHO cells -   10.1002/bit.22541.” Biotechnology and Bioengineering 105(2): 330-40. -   Delacote, F. and B. S. Lopez (2008). “Importance of the cell cycle     phase for the choice of the appropriate DSB repair pathway, for     genome stability maintenance: the trans-S double-strand break repair     model -   5149 [pii].” Cell Cycle 7(1): 33-8. -   Doudeva, L. G., H. Huang, et al. (2006). “Crystal structural     analysis and metal-dependent stability and activity studies of the     ColE7 endonuclease domain in complex with DNA/Zn2+ or     inhibitor/Ni2+15/2/269 [pii] 10.1110/ps.051903406.” Protein science:     a publication of the Protein Society 15(2): 269-80. -   Doyon, J. B., V. Pattanayak, et al. (2006). “Directed evolution and     substrate specificity profile of homing endonuclease I-SceI.”     Journal of the American Chemical Society 128(7): 2477-84. -   Doyon, J. B., V. Pattanayak, et al. (2006). “Directed evolution and     substrate specificity profile of homing endonuclease I-SceI.” J Am     Chem Soc 128(7): 2477-84. -   Doyon, Y., J. M. McCammon, et al. (2008). “Heritable targeted gene     disruption in zebrafish using designed zinc-finger nucleases -   nbt1409 [pii] 10.1038/nbt1409.” Nature Biotechnology 26(6): 702-8. -   Eastberg, J. H., J. Eklund, et al. (2007). “Mutability of an HNH     nuclease imidazole general base and exchange of a deprotonation     mechanism.” Biochemistry 46(24): 7215-25. -   Eisenschmidt, K., T. Lanio, et al. (2005). “Developing a programmed     restriction endonuclease for highly specific DNA cleavage.” Nucleic     Acids Res 33(22): 7039-47. -   Elrod-Erickson, M., M. A. Rould, et al. (1996). “Zif268 protein-DNA     complex refined at 1.6 A: a model system for understanding zinc     finger-DNA interactions.” Structure 4(10): 1171-80. -   Epinat, J. C., S. Arnould, et al. (2003). “A novel engineered     meganuclease induces homologous recombination in yeast and mammalian     cells.” Nucleic Acids Research 31(11): 2952-62. -   Epinat, J. C., S. Arnould, et al. (2003). “A novel engineered     meganuclease induces homologous recombination in yeast and mammalian     cells.” Nucleic Acids Res 31(11): 2952-62. -   Frank, K. M., J. M. Sekiguchi, et al. (1998). “Late embryonic     lethality and impaired V(D)J recombination in mice lacking DNA     ligase IV -   10.1038/24172.” Nature 396(6707): 173-7. -   Galetto, R., P. Duchateau, et al. (2009). “Targeted approaches for     gene therapy and the emergence of engineered meganucleases -   10.1517/14712590903213669.” Expert opinion on biological therapy     9(10): 1289-303. -   Gao, H., J. Smith, et al. (2010). “Heritable targeted mutagenesis in     maize using a designed endonuclease TP14041 [pii]     10.1111/j.1365-313X.2009.04041.x.” The Plant journal: for cell and     molecular biology 61(1): 176-87. -   Gao, Y., Y. Sun, et al. (1998). “A critical role for DNA end-joining     proteins in both lymphogenesis and neurogenesis -   S0092-8674(00)81714-6 [pii].” Cell 95(7): 891-902. -   Geurts, A. M., G. J. Cost, et al. (2009). “Knockout rats via embryo     microinjection of zinc-finger nucleases 325/5939/433 [pii]     10.1126/science.1172447.” Science 325(5939): 433. -   Gimble, F. S., C. M. Moure, et al. (2003). “Assessing the plasticity     of DNA target site recognition of the PI-SceI homing endonuclease     using a bacterial two-hybrid selection system.” J Mol Biol 334(5):     993-1008. -   Greisman, H. A. and C. O. Pabo (1997). “A general strategy for     selecting high-affinity zinc finger proteins for diverse DNA target     sites.” Science 275(5300): 657-61. -   Gruenert, D. C., E. Bruscia, et al. (2003). “Sequence-specific     modification of genomic DNA by small DNA fragments -   10.1172/JCI19773 112/5/637 [pii].” The Journal of clinical     investigation 112(5): 637-41. -   Guirouilh-Barbat, J., S. Huck, et al. (2004). “Impact of the KU80     pathway on NHEJ-induced genome rearrangements in mammalian cells.”     Mol Cell 14(5): 611-23. -   Guirouilh-Barbat, J., S. Huck, et al. (2004). “Impact of the KU80     pathway on NHEJ-induced genome rearrangements in mammalian cells -   10.1016/j.molce1.2004.05.008 S1097276504002916 [pii].” Molecular     Cell 14(5): 611-23. -   Guirouilh-Barbat, J., E. Rass, et al. (2007). “Defects in XRCC4 and     KU80 differentially affect the joining of distal nonhomologous     ends.” Proc Natl Acad Sci USA 104(52): 20902-7. -   Guirouilh-Barbat, J., E. Rass, et al. (2007). “Defects in XRCC4 and     KU80 differentially affect the joining of distal nonhomologous ends -   0708541104 [pii] 10.1073/pnas.0708541104.” Proceedings of the     National Academy of Sciences of the United States of America     104(52): 20902-7. -   Gurlebeck, D., B. Szurek, et al. (2005). “Dimerization of the     bacterial effector protein AvrBs3 in the plant cell cytoplasm prior     to nuclear import -   TPJ2370 [pii] 10.1111/j.1365-313X.2005.02370.x.” The Plant journal:     for cell and molecular biology 42(2): 175-87. -   Haber, J. (2000). “Partners and pathwaysrepairing a double-strand     break.” Trends Genet. 16(6): 259-264. -   Haber, J. E. (2008). “Alternative endings -   0711334105 [pii] 10.1073/pnas.0711334105.” Proceedings of the     National Academy of Sciences of the United States of America 105(2):     405-6. -   Hartsuiker, E., K. Mizuno, et al. (2009). “Ctp1CtIP and Rad32Mre11     nuclease activity are required for Rec12Spo11 removal, but     Rec12Spo11 removal is dispensable for other MRN-dependent meiotic     functions.” Mol Cell Biol 29(7): 1671-81. -   Hinnen, A., J. B. Hicks, et al. (1978). “Transformation of yeast.”     Proceedings of the National Academy of Sciences of the United States     of America 75(4): 1929-33. -   Hirata, R., J. Chamberlain, et al. (2002). “Targeted transgene     insertion into human chromosomes by adeno-associated virus vectors -   10.1038/nbt0702-735 nbt0702-735 [pii].” Nature Biotechnology 20(7):     735-8. -   Huang, H. and H. S. Yuan (2007). “The conserved asparagine in the     HNH motif serves an important structural role in metal finger     endonucleases.” Journal of Molecular Biology 368(3): 812-21. -   Ichiyanagi, K., Y. Ishino, et al. (2000). “Crystal structure of an     archaeal intein-encoded homing endonuclease PI-PfuI.” J Mol Biol     300(4): 889-901. -   Inoue, N., R. Dong, et al. (2001). “Introduction of single base     substitutions at homologous chromosomal sequences by     adeno-associated virus vectors -   10.1006/mthe.2001.0283 S1525-0016(01)90283-7 [pii].” Molecular     therapy: the journal of the American Society of Gene Therapy 3(4):     526-30. -   Isalan, M. and Y. Choo (2001). “Rapid, high-throughput engineering     of sequence-specific zinc finger DNA-binding proteins -   50076-6879(01)40444-7 [pii].” Methods in Enzymology 340: 593-609. -   Kalish, J. M. and P. M. Glazer (2005). “Targeted genome modification     via triple helix formation.” Ann N Y Acad Sci 1058: 151-61. -   Kim, H. J., H. J. Lee, et al. (2009). “Targeted genome editing in     human cells with zinc finger nucleases constructed via modular     assembly -   gr.089417.108 [pii] 10.1101/gr.089417.108.” Genome Research 19(7):     1279-88. -   Kim, Y. G., J. Cha, et al. (1996). “Hybrid restriction enzymes: zinc     finger fusions to Fok I cleavage domain.” Proceedings of the     National Academy of Sciences of the United States of America 93(3):     1156-60. -   Ku, W. Y., Y. W. Liu, et al. (2002). “The zinc ion in the HNH motif     of the endonuclease domain of colicin E7 is not required for DNA     binding but is essential for DNA hydrolysis.” Nucleic Acids Research     30(7): 1670-8. -   Landthaler, M., U. Begley, et al. (2002). “Two self-splicing group I     introns in the ribonucleotide reductase large subunit gene of     Staphylococcus aureus phage Twort.” Nucleic Acids Research 30(9):     1935-43. -   Landthaler, M., N. C. Lau, et al. (2004). “Group I intron homing in     Bacillus phages SPO₁ and SP82: a gene conversion event initiated by     a nicking homing endonuclease.” Journal of Bacteriology 186(13):     4307-14. -   Landthaler, M., B. W. Shen, et al. (2006). “I-BasI and I-HmuI: two     phage intron-encoded endonucleases with homologous DNA recognition     sequences but distinct DNA specificities.” Journal of Molecular     Biology 358(4): 1137-51. -   Landthaler, M. and D. A. Shub (2003). “The nicking homing     endonuclease I-BasI is encoded by a group I intron in the DNA     polymerase gene of the Bacillus thuringiensis phage Bastille.”     Nucleic Acids Research 31(12): 3071-7. -   Lee, S. E., F. Paques, et al. (1999). “Role of yeast SIR genes and     mating type in directing DNA double-strand breaks to homologous and     non-homologous repair paths.” Curr Biol 9(14): 767-70. -   Li, T., S. Huang, et al. (2010). “TAL nucleases (TALNs): hybrid     proteins composed of TAL effectors and FokI DNA-cleavage domain.”     Nucleic Acids Res 39(1): 359-72. -   Li, T., S. Huang, et al. (2011). “TAL nucleases (TALNs): hybrid     proteins composed of TAL effectors and FokI DNA-cleavage domain -   gkq704 [pii] 10.1093/nar/gkq704.” Nucleic Acids Research 39(1):     359-72. -   Liang, F., M. Han, et al. (1998). “Homology-directed repair is a     major double-strand break repair pathway in mammalian cells.”     Proceedings of the National Academy of Sciences of the United States     of America 95(9): 5172-7. -   Liu, P. Q., E. M. Chan, et al. (2010). “Generation of a triple-gene     knockout mammalian cell line using engineered zinc-finger nucleases -   10.1002/bit.22654.” Biotechnology and Bioengineering 106(1): 97-105. -   Liu, Q., J. T. Dansereau, et al. (2008). “Role of the interdomain     linker in distance determination for remote cleavage by homing     endonuclease I-TevI.” J Mol Biol 379(5): 1094-106. -   Liu, Q., V. Derbyshire, et al. (2006). “Distance determination by     GIY-YIG intron endonucleases: discrimination between repression and     cleavage functions.” Nucleic Acids Research 34(6): 1755-64. -   Lloyd, A., C. L. Plaisier, et al. (2005). “Targeted mutagenesis     using zinc-finger nucleases in Arabidopsis 0409339102 [pii]     10.1073/pnas.0409339102.” Proceedings of the National Academy of     Sciences of the United States of America 102(6): 2232-7. -   Maeder, M. L., S. Thibodeau-Beganny, et al. (2008). “Rapid     “open-source” engineering of customized zinc-finger nucleases for     highly efficient gene modification -   S1097-2765(08)00461-9 [pii] 10.1016/j.molcel.2008.06.016.” Molecular     Cell 31(2): 294-301. -   Mahfouz, M. M., L. Li, et al. (2011). “De novo-engineered     transcription activator-like effector (TALE) hybrid nuclease with     novel DNA binding specificity creates double-strand breaks -   1019533108 [pii] 10.1073/pnas.1019533108.” Proceedings of the     National Academy of Sciences of the United States of America 108(6):     2623-8. -   Marcaida, M. J., I. G. Munoz, et al. (2010). “Homing endonucleases:     from basics to therapeutic applications -   10.1007/s00018-009-0188-y.” Cellular and molecular life sciences:     CMLS 67(5): 727-48. -   Mashimo, T., A. Takizawa, et al. (2010). “Generation of knockout     rats with X-linked severe combined immunodeficiency (X-SCID) using     zinc-finger nucleases -   10.1371/journal.pone.0008870.” PloS one 5(1): e8870. -   McConnell Smith, A., R. Takeuchi, et al. (2009). “Generation of a     nicking enzyme that stimulates site-specific gene conversion from     the I-AniI LAGLIDADG homing endonuclease -   0810588106 [pii] 10.1073/pnas.0810588106.” Proceedings of the     National Academy of Sciences of the United States of America     106(13): 5099-104. -   McVey, M. and S. E. Lee (2008). “MMEJ repair of double-strand breaks     (director's cut): deleted sequences and alternative endings -   S0168-9525(08)00229-1 [pii] 10.1016/j.tig.2008.08.007.” Trends in     genetics: TIG 24(11): 529-38. -   Menoret, S., A. L. Iscache, et al. (2010). “Characterization of     immunoglobulin heavy chain knockout rats -   10.1002/eji.201040939.” European Journal of Immunology 40(10):     2932-41. -   Metzger, M. J., A. McConnell-Smith, et al. (2011). “Single-strand     nicks induce homologous recombination with less toxicity than     double-strand breaks using an AAV vector template -   gkq826 [pii] 10.1093/nar/gkq826.” Nucleic Acids Research 39(3):     926-35. -   Midon, M., P. Schafer, et al. (2011). “Mutational and biochemical     analysis of the DNA-entry nuclease EndA from Streptococcus     pneumoniae -   gkq802 [pii] 10.1093/nar/gkq802.” Nucleic Acids Research 39(2):     623-34. -   Miller, J. C., S. Tan, et al. (2011). “A TALE nuclease architecture     for efficient genome editing -   nbt.1755 [pii] 10.1038/nbt.1755.” Nature Biotechnology 29(2): 143-8. -   Mimitou, E. P. and L. S. Symington (2008). “Sae2, Exo1 and Sgs1     collaborate in DNA double-strand break processing.” Nature     455(7214): 770-4. -   Moore, I., M. Samalova, et al. (2006). “Transactivated and     chemically inducible gene expression in plants.” Plant J 45(4):     651-83. -   Moore, J. K. and J. E. Haber (1996). “Cell cycle and genetic     requirements of two pathways of nonhomologous end-joining repair of     double-strand breaks in Saccharomyces cerevisiae.” Mol Cell Biol     16(5): 2164-73. -   Moscou, M. J. and A. J. Bogdanove (2009). “A simple cipher governs     DNA recognition by TAL effectors.” Science 326(5959): 1501. -   Moscou, M. J. and A. J. Bogdanove (2009). “A simple cipher governs     DNA recognition by TAL effectors 1178817 [pii]     10.1126/science.1178817.” Science 326(5959): 1501. -   Moure, C. M., F. S. Gimble, et al. (2002). “Crystal structure of the     intein homing endonuclease PI-SceI bound to its recognition     sequence.” Nat Struct Biol 9(10): 764-70. -   Moure, C. M., F. S. Gimble, et al. (2003). “The crystal structure of     the gene targeting homing endonuclease I-SceI reveals the origins of     its target site specificity.” J Mol Biol 334(4): 685-95. -   Nimonkar, A. V., J. Genschel, et al. (2011). “BLM-DNA2-RPA-MRN and     EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for     human DNA break repair.” Genes Dev 25(4): 350-62. -   Niu, Y., K. Tenney, et al. (2008). “Engineering variants of the     I-SceI homing endonuclease with strand-specific and site-specific     DNA-nicking activity -   S0022-2836(08)00840-1 [pii] 10.1016/j.jmb.2008.07.010.” Journal of     Molecular Biology 382(1): 188-202. -   Orr-Weaver, T. L., J. W. Szostak, et al. (1981). “Yeast     transformation: a model system for the study of recombination.”     Proceedings of the National Academy of Sciences of the United States     of America 78(10): 6354-8. -   Orr-Weaver, T. L., J. W. Szostak, et al. (1983). “Genetic     applications of yeast transformation with linear and gapped     plasmids.” Methods in Enzymology 101: 228-45. -   Pabo, C. O., E. Peisach, et al. (2001). “Design and selection of     novel Cys2H is2 zinc finger proteins -   70/1/313 [pii] 10.1146/annurev.biochem. 70.1.313.” Annual Review of     Biochemistry 70: 313-40. -   Padidam, M. (2003). “Chemically regulated gene expression in     plants.” Curr Opin Plant Biol 6(2): 169-77. -   Paques, F. and P. Duchateau (2007). “Meganucleases and DNA     double-strand break-induced recombination: perspectives for gene     therapy.” Current Gene Therapy 7(1): 49-66. -   Paques, F. and P. Duchateau (2007). “Meganucleases and DNA     double-strand break-induced recombination: perspectives for gene     therapy.” Curr Gene Ther 7(1): 49-66. -   Paques, F. and J. E. Haber (1999). “Multiple pathways of     recombination induced by double-strand breaks in Saccharomyces     cerevisiae.” Microbiology and molecular biology reviews: MMBR 63(2):     349-404. -   Perez, E. E., J. Wang, et al. (2008). “Establishment of HIV-1     resistance in CD4+ T cells by genome editing using zinc-finger     nucleases -   nbt1410 [pii] 10.1038/nbt1410.” Nature Biotechnology 26(7): 808-16. -   Pierce, A. J., P. Hu, et al. (2001). “Ku DNA end-binding protein     modulates homologous repair of double-strand breaks in mammalian     cells.” Genes Dev 15(24): 3237-42. -   Pingoud, A. and G. H. Silva (2007). “Precision genome surgery.” Nat     Biotechnol 25(7): 743-4. -   Porteus, M. H. and D. Carroll (2005). “Gene targeting using zinc     finger nucleases.” Nat Biotechnol 23(8): 967-73. -   Ramirez, C. L., J. E. Foley, et al. (2008). “Unexpected failure     rates for modular assembly of engineered zinc fingers -   nmeth0508-374 [pii] 10.1038/nmeth0508-374.” Nature Methods 5(5):     374-5. -   Rosen, L. E., H. A. Morrison, et al. (2006). “Homing endonuclease     I-CreI derivatives with novel DNA target specificities.” Nucleic     Acids Research 34(17): 4791-800. -   Rosen, L. E., H. A. Morrison, et al. (2006). “Homing endonuclease     I-CreI derivatives with novel DNA target specificities.” Nucleic     Acids Res. -   Rothstein, R. J. (1983). “One-step gene disruption in yeast.”     Methods in Enzymology 101: 202-11. -   Rouet, P., F. Smih, et al. (1994). “Expression of a site-specific     endonuclease stimulates homologous recombination in mammalian     cells.” Proc Natl Acad Sci USA 91(13): 6064-8. -   Rouet, P., F. Smih, et al. (1994). “Introduction of double-strand     breaks into the genome of mouse cells by expression of a     rare-cutting endonuclease.” Mol Cell Biol 14(12): 8096-106. -   Russell, D. W. and R. K. Hirata (1998). “Human gene targeting by     viral vectors -   10.1038/ng0498-325.” Nature Genetics 18(4): 325-30. -   Sangiuolo, F., M. L. Scaldaferri, et al. (2008). “Cftr gene     targeting in mouse embryonic stem cells mediated by Small Fragment     Homologous Replacement (SFHR) 2904 [pii].” Frontiers in bioscience:     a journal and virtual library 13: 2989-99. -   Santiago, Y., E. Chan, et al. (2008). “Targeted gene knockout in     mammalian cells by using engineered zinc-finger nucleases -   0800940105 [pii] 10.1073/pnas.0800940105.” Proceedings of the     National Academy of Sciences of the United States of America     105(15): 5809-14. -   Sartori, A. A., C. Lukas, et al. (2007). “Human CtIP promotes DNA     end resection.” Nature 450(7169): 509-14. -   Seligman, L. M., K. M. Chisholm, et al. (2002). “Mutations altering     the cleavage specificity of a homing endonuclease.” Nucleic Acids     Research 30(17): 3870-9. -   Seligman, L. M., K. M. Stephens, et al. (1997). “Genetic analysis of     the Chlamydomonas reinhardtii I-CreI mobile intron homing system in     Escherichia coli.” Genetics 147(4): 1653-64. -   Shen, B. W., M. Landthaler, et al. (2004). “DNA binding and cleavage     by the HNH homing endonuclease I-HmuI.” Journal of Molecular Biology     342(1): 43-56. -   Shukla, V. K., Y. Doyon, et al. (2009). “Precise genome modification     in the crop species Zea mays using zinc-finger nucleases -   nature07992 [pii] 10.1038/nature07992.” Nature 459(7245): 437-41. -   Silva, G. H., J. Z. Dalgaard, et al. (1999). “Crystal structure of     the thermostable archaeal intron-encoded endonuclease I-DmoI.” J Mol     Biol 286(4): 1123-36. -   Simon, P., F. Cannata, et al. (2008). “Sequence-specific DNA     cleavage mediated by bipyridine polyamide conjugates.” Nucleic Acids     Res 36(11): 3531-8. -   Smith, J., J. M. Berg, et al. (1999). “A detailed study of the     substrate specificity of a chimeric restriction enzyme -   gkc139 [pii].” Nucleic Acids Research 27(2): 674-81. -   Smith, J., M. Bibikova, et al. (2000). “Requirements for     double-strand cleavage by chimeric restriction enzymes with zinc     finger DNA-recognition domains.” Nucleic Acids Research 28(17):     3361-9. -   Smith, J., S. Grizot, et al. (2006). “A combinatorial approach to     create artificial homing endonucleases cleaving chosen sequences.”     Nucleic Acids Research 34(22): e149. -   Smith, J., S. Grizot, et al. (2006). “A combinatorial approach to     create artificial homing endonucleases cleaving chosen sequences.”     Nucleic Acids Res 34(22): e149. -   Sonoda, E., H. Hochegger, et al. (2006). “Differential usage of     non-homologous end-joining and homologous recombination in double     strand break repair.” DNA Repair (Amst) 5(9-10): 1021-9. -   Spiegel, P. C., B. Chevalier, et al. (2006). “The structure of     I-CeuI homing endonuclease: Evolving asymmetric DNA recognition from     a symmetric protein scaffold.” Structure 14(5): 869-80. -   Stoddard, B. L. (2005). “Homing endonuclease structure and     function.” Quarterly Reviews of Biophysics 38(1): 49-95. -   Stoddard, B. L. (2005). “Homing endonuclease structure and     function.” Q Rev Biophys 38(1): 49-95. -   Stoddard, B. L., A. M. Scharenberg, et al. (2007). Advances in     Engineering Homing Endonucleases for Gene Targeting Ten Years After     Structures. Progress in Gene Therapy: Autologous and Cancer Stem     Cell Gene Therapy. R. Bertolotti and K. Ozawa, World Scientific     Publishing Co. Pte. Ltd. 3: 135-68. -   Sugawara, N. and J. E. Haber (1992). “Characterization of     double-strand break-induced recombination: homology requirements and     single-stranded DNA formation.” Mol Cell Biol 12(2): 563-75. -   Sun, H., D. Treco, et al. (1991). “Extensive 3′-overhanging,     single-stranded DNA associated with the meiosis-specific     double-strand breaks at the ARG4 recombination initiation site.”     Cell 64(6): 1155-61. -   Sussman, D., M. Chadsey, et al. (2004). “Isolation and     characterization of new homing endonuclease specificities at     individual target site positions.” Journal of Molecular Biology     342(1): 31-41. -   Sussman, D., M. Chadsey, et al. (2004). “Isolation and     characterization of new homing endonuclease specificities at     individual target site positions.” J Mol Biol 342(1): 31-41. -   Taubes, G. (2002). “Gene therapy. The strange case of chimeraplasty -   10.1126/science.298.5601.2116 298/5601/2116 [pii].” Science     298(5601): 2116-20. -   Wang, R., X. Zhou, et al. (2003). “Chemically regulated expression     systems and their applications in transgenic plants.” Transgenic Res     12(5): 529-40. -   Wang, Y. T., J. D. Wright, et al. (2009). “Redesign of high-affinity     nonspecific nucleases with altered sequence preference -   10.1021/ja907160r.” Journal of the American Chemical Society     131(47): 17345-53. -   White, C. I. and J. E. Haber (1990). “Intermediates of recombination     during mating type switching in Saccharomyces cerevisiae.” Embo J     9(3): 663-73. -   Yang, M., V. Djukanovic, et al. (2009). “Targeted mutagenesis in the     progeny of maize transgenic plants -   10.1007/s11103-009-9499-5.” Plant Molecular Biology 70(6): 669-79. -   Zhao, L., R. P. Bonocora, et al. (2007). “The restriction fold turns     to the dark side: a bacterial homing endonuclease with a PD-(D/E)-XK     motif.” The EMBO Journal 26(9): 2432-42. -   Zuo, J. and N. H. Chua (2000). “Chemical-inducible systems for     regulated expression of plant genes.” Curr Opin Biotechnol 11(2):     146-51.

MEGA 

The invention claimed is:
 1. A compact Transcription Activator-Like Effector Nuclease (TALEN) monomer comprising: (i) one core TALE scaffold comprising Repeat Variable Dipeptide regions (RVDs) having DNA binding specificity onto a specific double-stranded DNA target sequence of interest; and (ii) at least one I-TevI nuclease domain, wherein said I-TevI nuclease domain consists essentially of: (a) amino acids 1-196 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-196 of SEQ ID NO: 20; (b) amino acids 1-183 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-183 of SEQ ID NO: 20; (c) amino acids 1-169 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-169 of SEQ ID NO: 20; (d) amino acids 1-148 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-148 of SEQ ID NO: 20; or (e) amino acids 1-123 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-123 of SEQ ID NO: 20; wherein said I-TevI nuclease domain is capable of cleaving DNA a few base pairs away from said double-stranded DNA target sequence of interest when fused to the C-terminus or N-terminus of said core TALE scaffold from (i); wherein said compact TALEN monomer is assembled to bind said target DNA sequence and cleave double-stranded DNA without requiring dimerization.
 2. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain is fused to the C-terminus of said core TALE scaffold.
 3. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain is fused to the N-terminus of said core TALE scaffold.
 4. A compact TALEN monomer according to claim 1, wherein (i) said I-TevI nuclease domain is fused to the C-terminus and another nuclease domain is fused to the N-terminus of said core TALE scaffold; (ii) said I-TevI nuclease domain is fused to the N-terminus and another nuclease domain is fused to the C-terminus and of said core TALE scaffold; or (iii) said I-TevI nuclease domain is fused to the N-terminus and C terminus and of said core TALE scaffold.
 5. A compact TALEN monomer according to claim 1, comprising a protein sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with a protein sequence selected from the group consisting of SEQ ID NO: 426-432.
 6. A compact TALEN monomer according to claim 1, wherein said core TALE scaffold comprises a protein sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with a protein sequence selected from the group consisting of SEQ ID NO: 134 and SEQ ID NO:
 135. 7. A compact TALEN monomer according to claim 1, wherein said core TALE scaffold comprises a protein sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with a protein sequence selected from the group consisting of SEQ ID NO: 136 to SEQ ID NO:
 139. 8. A compact TALEN monomer according to claim 1, wherein said compact TALEN further comprises a peptidic linker sequence to fuse said I-TevI nuclease domain to said core TALE scaffold, said peptidic linker selected from the group consisting of SEQ ID NO: 67-104 and SEQ ID NO: 372-415.
 9. A compact TALEN monomer according to claim 1, comprising a protein sequence selected from the group consisting of SEQ ID NO: 448 and
 450. 10. A compact TALEN monomer according to claim 8, wherein said another nuclease domain is selected from the group consisting of a ColE7 domain, a NucA domain, and a FokI domain.
 11. A compact TALEN according to claim 1, comprising a protein sequence selected from the group consisting of SEQ ID NO: 447-450.
 12. A recombinant polynucleotide encoding a compact TALEN according to any one of claims 1, 2-4, 5, 6, 7, 8, and 9-11.
 13. A vector comprising a recombinant polynucleotide according to claim
 12. 14. A composition comprising a compact TALEN according to any one of claims 1, 2-4, 5, 6, 7, 8, and 9-11 and a carrier.
 15. An isolated host cell which comprises a recombinant polynucleotide of claim
 12. 16. A kit comprising a compact TALEN monomer according to any one of claims 1, 2-4, 5, 6, 7, 8, and 9-11 and instructions for use in enhancing DNA cleavage efficiency of a double-stranded DNA.
 17. A compact TALEN monomer according claim 1, wherein said compact TALEN further comprises a peptidic linker sequence to fuse said I-TevI catalytic domain to said core TALE scaffold.
 18. A compact TALEN monomer according to claim 1, wherein said nuclease domain consists essentially of: amino acids 1-196 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-196 of SEQ ID NO:
 20. 19. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain consists essentially of: amino acids 1-183 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-183 of SEQ ID NO:
 20. 20. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain consists essentially of: amino acids 1-169 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-169 of SEQ ID NO:
 20. 21. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain consists essentially of: amino acids 1-148 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-148 of SEQ ID NO:
 20. 22. A compact TALEN monomer according to claim 1, wherein said I-TevI nuclease domain consists essentially of: amino acids 1-123 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-123 of SEQ ID NO:
 20. 23. A method for cleaving a double-stranded DNA, comprising: (a) selecting one DNA target sequence of interest on one strand of a double-stranded DNA; (b) providing a compact TALEN monomer comprising: (i) one core TALE scaffold comprising Repeat Variable Dipeptide regions (RVDs) having DNA binding specificity onto the DNA target sequence of interest; and (ii) at least one I-TevI nuclease domain, wherein said I-TevI nuclease domain consists essentially of: (a) amino acids 1-196 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-196 of SEQ ID NO: 20; (b) amino acids 1-183 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-183 of SEQ ID NO: 20; (c) amino acids 1-169 of SEQ ID NO:20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-169 of SEQ ID NO: 20; (d) amino acids 1-148 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-148 of SEQ ID NO: 20; or (e) amino acids 1-123 of SEQ ID NO: 20; or an amino acid sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with amino acids 1-123 of SEQ ID NO: 20; wherein said I-TevI nuclease domain is capable of cleaving DNA a few base pairs away from said double-stranded DNA target sequence of interest when fused to the C-terminus or N-terminus of said core TALE scaffold from (i); wherein said compact TALEN monomer is assembled to bind and cleave said double stranded DNA without requiring dimerization; and (c) contacting said double-stranded DNA with said compact TALEN monomer such that the double-stranded DNA is cleaved a few base pairs away in 3′ and/or 5′ direction(s) from said DNA target sequence of interest.
 24. A method according to claim 23, wherein said I-TevI nuclease domain is fused to the C-terminus of said core TALE scaffold.
 25. A method according to claim 23, wherein said I-TevI nuclease domain is fused to the N-terminus of said core TALE scaffold.
 26. A method according to claim 23, wherein said I-TevI nuclease domain is fused to the C-terminus and N-terminus of of said core TALE scaffold.
 27. A method according to claim 23, wherein said core TALE scaffold comprises a protein sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with a protein sequence selected from the group consisting of SEQ ID NO: 134 and SEQ ID NO:
 135. 28. A method according to claim 23, wherein said core TALE scaffold comprises a protein sequence having at least 80%, at least 90%, or at least 95% amino acid sequence identity with a protein sequence selected from the group consisting of SEQ ID NO: 136 to SEQ ID NO:
 139. 29. A method according to of claim 23, wherein said compact TALEN monomer further comprises a peptidic linker sequence to fuse said I-TevI nuclease domain to said core TALE scaffold, wherein said peptidic linker sequence is selected from the group consisting of SEQ ID NO: 67-104 and SEQ ID NO: 372-415.
 30. A method according to claim 23, wherein said compact TALEN monomer comprises a protein sequence selected from the group consisting of SEQ ID NO: 448 and
 450. 31. A method according to claim 23, wherein said compact TALEN monomer comprises a protein sequence selected from the group consisting of SEQ ID NO: 447-450.
 32. A method according claim 1, wherein (i) said I-TevI nuclease domain is fused to the C-terminus and another nuclease domain is fused to the N-terminus of said core TALE scaffold; (ii) said I-TevI nuclease domain is fused to the N-terminus and another nuclease domain is fused to the C-terminus and of said core TALE scaffold; or (iii) said I-TevI nuclease domain is fused to the N-terminus and C-terminus and of said core TALE scaffold.
 33. A method according to claim 32, wherein said another nuclease domain is selected from the group consisting of a ColE7 domain, a NucA domain, and a FokI domain. 